Data / Medical devices / United States / Wells Johnson Co.
Wells Johnson Co.: FDA-registered device maker in Tucson, AZ, United States, 2 510(k) clearances
Wells Johnson Co. is registered with the FDA (registration 2024022) in Tucson, AZ, United States. It lists 6 device types. The FDA files 2 510(k) clearances under its listings, the newest dated August 30, 1999. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2024022
- Address
- 8000 S Kolb Rd, Tucson, AZ, United States, 85756
- Owner or operator
- WELLS JOHNSON CO. (2024022)
- Roles
- Manufacturer, Specification developer
- First device listed
- June 15, 1992
- Registered through
- 2026
- Brand names listed
- 'Y' Small Bore Infiltration Tubing, 1 Hole Standard Cannula, 10cc, 35cc ,60cc Punch Awls, 10cc, 35cc 60cc Clicker lock, 10cc, 35cc, 60cc Back Plug Stainless steel & Black Delrin, 10cc, 35cc, 60cc Female Toomey Transfer Hub, 10cc, 35cc, 60cc Male Toomey Transfer Hub, 10cc,35cc,60cc Horseshoe Lock and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bottle, Collection, Vacuum | KDQ | 2 | Manufacturer | accessdata.fda.gov |
| Cannula, Surgical, General & Plastic Surgery | GEA | 1 | Manufacturer | accessdata.fda.gov |
| Pump, Infusion | FRN | 2 | Manufacturer | accessdata.fda.gov |
| Pump, Portable, Aspiration (Manual Or Powered) | BTA | 2 | Manufacturer | accessdata.fda.gov |
| Stand, Infusion | FOX | 1 | Manufacturer | accessdata.fda.gov |
| Tubing, Noninvasive | GAZ | 2 | 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 |
|---|---|---|---|---|---|---|
| August 30, 1999 | K991437 | WELLS JOHNSON INFUSION SYSTEM, MODEL 20-6000-00 | FRN | Substantially Equivalent | Wells Johnson Co. | accessdata.fda.gov |
| October 20, 1983 | K832274 | ASPIRATOR | BTA | Substantially Equivalent | Wells Johnson Co. | accessdata.fda.gov |
Compare with other makers
- All makers of Stand, Infusion
- All makers of Pump, Portable, Aspiration (Manual Or Powered)
- All makers of Cannula, Surgical, General & Plastic Surgery
- All makers of Pump, Infusion
- All makers of Tubing, Noninvasive
- All makers of Bottle, Collection, Vacuum
Updated August 30, 1999. 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.