Data / Medical devices / United States / Nutra-Med Packaging LLC.
Nutra-Med Packaging LLC.: FDA-registered device maker in East Hanover, NJ, United States, 2 510(k) clearances
Nutra-Med Packaging LLC. is registered with the FDA (registration 3002821211) in East Hanover, NJ, United States. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated November 15, 2018. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3002821211
- Address
- 601 Murray Rd, East Hanover, NJ, United States, 07936
- Owner or operator
- Nutra-Med Packaging LLC. (10081914)
- Roles
- Repackager or relabeler
- First device listed
- May 26, 2021
- Registered through
- 2026
- Brand names listed
- Sitzmarks
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Coronavirus Antigen Detection Test System. | QKP | N | Repackager or relabeler | accessdata.fda.gov |
| System, Gastrointestinal Motility (Electrical) | FFX | 2 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| November 15, 2018 | K181750 | SITZMARKS | FFX | Substantially Equivalent | Konsyl Pharmaceuticals | accessdata.fda.gov |
| July 8, 1988 | K881609 | SITZMARKS | FFX | Substantially Equivalent | Lafayette Pharmacal, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of System, Gastrointestinal Motility (Electrical)
- All makers of Coronavirus Antigen Detection Test System.
Updated November 15, 2018. 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.