Data / Medical devices / United States / Preferred Medical Products, LLC
Preferred Medical Products, LLC: FDA-registered device maker in Copperhill, TN, United States, 2 510(k) clearances
Preferred Medical Products, LLC is registered with the FDA (registration 1038913) in Copperhill, TN, United States. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated March 14, 1989. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1038913
- Address
- 191 Industrial DR, Copperhill, TN, United States, 37317
- Owner or operator
- PREFERRED MEDICAL PRODUCTS (1038913)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- December 19, 2007
- Registered through
- 2026
- Brand names listed
- Bag Decanter, Equipment Covers, Waste Pouch
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Container, I.V. | KPE | 2 | Manufacturer | accessdata.fda.gov |
| Instrument, Surgical, Disposable | KDC | 1 | Contract manufacturer | accessdata.fda.gov |
| System, X-Ray, Fluoroscopic, Image-Intensified | JAA | 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 |
|---|---|---|---|---|---|---|
| March 14, 1989 | K890272 | BAG DECANTER | KPE | Substantially Equivalent | Superior Medical Products | accessdata.fda.gov |
| March 6, 1987 | K863853 | EAZY COVERS | JAA | Substantially Equivalent | Superior Medical Products | accessdata.fda.gov |
Compare with other makers
- All makers of Container, I.V.
- All makers of System, X-Ray, Fluoroscopic, Image-Intensified
- All makers of Instrument, Surgical, Disposable
Updated March 14, 1989. 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.