Data / Medical devices / United States / Prima Care Medical Supplies, Inc.
Prima Care Medical Supplies, Inc.: FDA-registered device maker in Paterson, NJ, United States, 2 510(k) clearances
Prima Care Medical Supplies, Inc. is registered with the FDA (registration 3005616800) in Paterson, NJ, United States. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated July 2, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3005616800
- Address
- 239 6th Ave, Paterson, NJ, United States, 07524
- Owner or operator
- Prima-Care Medical Supplies, Inc. (10039985)
- Roles
- Repackager or relabeler
- First device listed
- March 11, 2013
- Registered through
- 2026
- Brand names listed
- ANEROID, Dressing, SPHYGMOMANOMETER
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Blood Pressure Cuff | DXQ | 2 | Repackager or relabeler | accessdata.fda.gov |
| Dressing, Wound, Hydrophilic | NAC | 1 | Repackager or relabeler | accessdata.fda.gov |
| Stethoscope, Manual | LDE | 1 | 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 |
|---|---|---|---|---|---|---|
| July 2, 2020 | K193259 | Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer | DXQ | Substantially Equivalent | Little Doctor Electronic (Nantong)Co.,Ltd | accessdata.fda.gov |
| December 1, 2008 | K082208 | DOCTORS CHOICE SLOW HEALING BANDAGE WITH SPRAY ON REMOVER | NAC | Substantially Equivalent | Scivolutions, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Dressing, Wound, Hydrophilic
- All makers of Stethoscope, Manual
- All makers of Blood Pressure Cuff
Updated July 2, 2020. 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.