Data / Medical devices / United States / Reprocessing Products Corporation (RPC)
Reprocessing Products Corporation (RPC): FDA-registered device maker in Tucson, AZ, United States, 15 510(k) clearances
Reprocessing Products Corporation (RPC) is registered with the FDA (registration 2028411) in Tucson, AZ, United States. It lists 30 device types. The FDA files 15 510(k) clearances under its listings, the newest dated October 18, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2028411
- FEI number
- 1000125241
- Address
- 1643 W Modern Ct, Tucson, AZ, United States, 85705
- Owner or operator
- REPROCESSING PRODUCTS CORPORATION (RPC) (9004570)
- Roles
- Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer
- First device listed
- September 4, 2002
- Registered through
- 2026
- Brand names listed
- 1 mS NaCl Conductivity Solution - S-0021 - 500mL, 10 pH Buffer Solution 500mL - S-0013, 10" 0.2 Micron - PPPG10H100022, 10" 0.2 Micron PES - 25103100021WG, 10" 0.2 Micron PES - 2510H100021WG, 10" 0.2 Micron PP - PG10H100021, 10" 0.2 mic Vent PTFE - 34103100021G, 10" 0.5 Mic CBC - AM-155162 - 12/case and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessory, Surgical Apparel | LYU | 1 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Agent, Chelating For Decalcification | KDY | 1 | Complaint file establishment, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Analyzer, Gas, Water Vapor, Gaseous-Phase | BXA | 1 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Blood Pressure Cuff | DXQ | 2 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Bottle, Hot/Cold Water | FPF | 1 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Clamp, Dialysis Arm | NOO | 1 | Complaint file establishment, Manufacturer, Specification developer | accessdata.fda.gov |
| Clamp, Non-Electrical | FFN | 1 | Complaint file establishment, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Container, Specimen, Non-Sterile | NNI | 1 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Detector, Leak, Blood | FJD | 2 | Complaint file establishment, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Dialyzer Reprocessing System | LIF | 2 | Complaint file establishment, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Dialyzer, Capillary, Hollow Fiber | FJI | 2 | Complaint file establishment, Manufacturer, Specification developer | accessdata.fda.gov |
| Filter, Blood, Dialysis | FKJ | 2 | Repackager or relabeler | accessdata.fda.gov |
| Forceps | HTD | 1 | Complaint file establishment, Manufacturer, Specification developer | accessdata.fda.gov |
| Formulations, Balanced Salt Solutions | KIP | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Label Or Tag, Non-Sterile | QMX | 1 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Ph Buffer | JCC | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Purifier, Water (Absorption, Deionization, Membrane Filter, Reverse Osmosis) | JRS | 1 | Complaint file establishment, Manufacturer, Specification developer | accessdata.fda.gov |
| Purifier, Water, Ultraviolet, Medical | KMG | 2 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Set, Dialyzer Holder | FKI | 2 | Complaint file establishment, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Set, Tubing, Blood, With And Without Anti-Regurgitation Valve | FJK | 2 | Complaint file establishment, Manufacturer, Specification developer | accessdata.fda.gov |
| Solution, Decalcifier, Acid Containing | KDX | 1 | Complaint file establishment, Manufacturer, Specification developer | accessdata.fda.gov |
| Sterilant, Medical Devices | MED | 2 | Repackager or relabeler | accessdata.fda.gov |
| Strip, Dialysate Ph Indicator | MNV | 2 | Complaint file establishment, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Strip, Test, Reagent, Residuals For Dialysate, Disinfectant | MSY | 2 | Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| System, Hemodialysis, Remote Accessories | MON | 1 | Complaint file establishment, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Test, Urine Leukocyte | LJX | 1 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Tie, Dialysis | FKE | 1 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Tubing, Pressure And Accessories | BYX | 1 | Complaint file establishment, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Unit, Filter, Membrane | JRL | 1 | Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 18, 2022 | K222167 | E-Z Chek Chlorine Residual Test Strips (K100-0101B) | MSY | Substantially Equivalent | Reprocessing Products Corporation (Rpc) | accessdata.fda.gov |
| December 19, 2017 | K171889 | Reusable Blood Pressure Cuff | DXQ | Substantially Equivalent | Suzhou Minhua Medical Apparatus Supplies Co., Ltd. | accessdata.fda.gov |
| February 25, 2014 | K132344 | E-Z CHECK OZONE TEST STRIPS | MSY | Substantially Equivalent | Reprocessing Products Corporation (Rpc) | accessdata.fda.gov |
| March 20, 2013 | K123805 | E-Z CHEK BLOOD LEAK TEST STRIPS | FJD | Substantially Equivalent | Reprocessing Products Corp | accessdata.fda.gov |
| January 7, 2011 | K101750 | RPC E-Z CHEK 6.8-8.5 PH TEST STRIPS, MODEL K100-0117 AND E-Z CHEK 0-14 PH TEST STRIPS, MODEL K100-0104 | MNV | Substantially Equivalent | Reprocessing Products Corp | accessdata.fda.gov |
| May 8, 2009 | K090338 | ULTRA LOW TOTAL CHLORINE, E-Z CHEK SENSITIVE TOTAL CHLORINE | MSY | Substantially Equivalent | Reprocessing Products Corp | accessdata.fda.gov |
| May 5, 2000 | K000578 | SERIM LEUKOCYTE ESTERASE TEST STRIPS | LJX | Substantially Equivalent | Serim Research Corp. | accessdata.fda.gov |
| February 10, 1999 | K974426 | POTENCY TEST STRIPS, INDICATOR TEST STRIPS | LIF | Substantially Equivalent | Reprocessing Products Corp | accessdata.fda.gov |
| December 7, 1998 | K974064 | MICRO X RESIDUAL TEST STRIPS | MSY | Substantially Equivalent | Reprocessing Products Corp | accessdata.fda.gov |
| June 5, 1998 | K962959 | PERACIDIN DIALYZER REPROCESSING CONCENTRATE | MED | Substantially Equivalent | Hdc Medical, Inc. | accessdata.fda.gov |
| November 30, 1995 | K950602 | PORT CAPS (PROTECTIVE CLOSURES FOE REPROCESSED HEMODIALYZERS | FJI | Substantially Equivalent | Reprocessing Products Corp | accessdata.fda.gov |
| February 22, 1994 | K940214 | STATCORP INC. DISPOSABLE BLOOD PRESSURE CUFF | DXQ | Substantially Equivalent | Statcorp, Inc. | accessdata.fda.gov |
| September 13, 1990 | K901734 | SERIM RESIDUAL CHLORINE TEST KIT | FKJ | Substantially Equivalent | Serim Research Corp. | accessdata.fda.gov |
| July 29, 1985 | K852605 | BLOOD TUBING SET | FJK | Substantially Equivalent | Medflex International, Inc. | accessdata.fda.gov |
| March 29, 1983 | K830574 | RENATRON DIALYZER REPROCESSING SYS | LIF | Substantially Equivalent | Renal Systems, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Strip, Test, Reagent, Residuals For Dialysate, Disinfectant
- All makers of Bottle, Hot/Cold Water
- All makers of Clamp, Dialysis Arm
- All makers of Unit, Filter, Membrane
- All makers of Analyzer, Gas, Water Vapor, Gaseous-Phase
- All makers of Purifier, Water (Absorption, Deionization, Membrane Filter, Reverse Osmosis)
Updated October 18, 2022. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.