Data / Medical devices / United States / NBS Group Supply- Medical Products Division, LLC
NBS Group Supply- Medical Products Division, LLC: FDA-registered device maker in New Brunswick, NJ, United States, 1 510(k) clearance
NBS Group Supply- Medical Products Division, LLC is registered with the FDA (registration 2249651) in New Brunswick, NJ, United States. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 14, 2000. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2249651
- FEI number
- 3002771993
- Address
- 257 Livingston Ave., New Brunswick, NJ, United States, 08901
- Owner or operator
- NBS GROUP SUPPLY- MEDICAL PRODUCTS DIVISION, LLC (9040634)
- Roles
- Specification developer
- First device listed
- January 6, 2012
- Registered through
- 2026
- Brand names listed
- Storz Disp High Flow Insufflation Tbg w/Filter #20400161S, Storz Disp High Flow Insufflation Tbg w/Filter #20400162S
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Apparatus, Suction, Ward Use, Portable, Ac-Powered | JCX | 2 | Specification developer | accessdata.fda.gov |
| Collector, Urine, (And Accessories) For Indwelling Catheter | KNX | 2 | Specification developer | accessdata.fda.gov |
| Insufflator, Laparoscopic | HIF | 2 | Specification developer | accessdata.fda.gov |
| Laparoscope, General & Plastic Surgery | GCJ | 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 |
|---|---|---|---|---|---|---|
| June 14, 2000 | K001068 | NBS CONNECTING TUBE SET | HIF | Substantially Equivalent | Nbs Products CO | accessdata.fda.gov |
Compare with other makers
- All makers of Apparatus, Suction, Ward Use, Portable, Ac-Powered
- All makers of Collector, Urine, (And Accessories) For Indwelling Catheter
- All makers of Laparoscope, General & Plastic Surgery
- All makers of Insufflator, Laparoscopic
Updated June 14, 2000. 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.