Data / Medical devices / United States / Norfolk Medical Products, Inc.
Norfolk Medical Products, Inc.: FDA-registered device maker in Skokie, IL, United States, 5 510(k) clearances
Norfolk Medical Products, Inc. is registered with the FDA (registration 1450392) in Skokie, IL, United States. It lists 4 device types. The FDA files 5 510(k) clearances under its listings, the newest dated August 20, 2015. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 1450392
- Address
- 7350 North Ridgeway, Skokie, IL, United States, 60076
- Owner or operator
- NORFOLK MEDICAL PRODUCTS, INC. (1450392)
- Roles
- Manufacturer, Repackager or relabeler, Specification developer
- First device listed
- September 16, 1992
- Registered through
- 2026
- Brand names listed
- Clear-View Set, ClearView Set/ClearView-MS Set/Aqua-C Hydration System, NorPort, Norport, POSI GRIP NEEDLE, Tidal High-Flow Non-coring Needle, TidalPort
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Needle, Aspiration And Injection, Disposable | GAA | 1 | Manufacturer | accessdata.fda.gov |
| Needle, Hypodermic, Single Lumen | FMI | 2 | Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Port & Catheter, Implanted, Subcutaneous, Intravascular | LJT | 2 | Manufacturer | accessdata.fda.gov |
| Set, Administration, Intravascular | FPA | 2 | Manufacturer | 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 20, 2015 | K151341 | Turbo High-Flow Non-coring Needle | FMI | Substantially Equivalent | Norfolk Medical | accessdata.fda.gov |
| October 27, 2011 | K112713 | NORFOLK MEDICAL-SPORTPORT-FAMILY OF PORTS | LJT | Substantially Equivalent | Norfolk Medical Products, Inc. | accessdata.fda.gov |
| August 25, 2011 | K111101 | NORPORT CT-PC, LUCENT NON-CORING NEEDEL INFUSION SET | LJT | Substantially Equivalent | Norfolk Medical | accessdata.fda.gov |
| January 14, 2011 | K102385 | NORFOLK MEDICAL NORPORT FAMILY OF PORTS | LJT | Substantially Equivalent | Norfolk Medical Products, Inc. | accessdata.fda.gov |
| February 10, 1987 | K870188 | NORFOLK MEDICAL BUTTERFLY INFUSION SET | FPA | Substantially Equivalent | Norfolk Medical Products, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Needle, Aspiration And Injection, Disposable
- All makers of Port & Catheter, Implanted, Subcutaneous, Intravascular
- All makers of Set, Administration, Intravascular
- All makers of Needle, Hypodermic, Single Lumen
Updated August 20, 2015. 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.