FDA Device Establishments · JSON-LD · Markdown
FEI 3007478714 · Repack or Relabel Medical Device · Status: Active
| FEI Number | 3007478714 |
|---|---|
| Owner / Operator | Precision Medical Devices (#9098188) |
| Address | 121 Jersey Ave, Suite 203, New Brunswick, NJ, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | KNX |
| Regulation § (21 CFR) | 876.5250 |
| Proprietary names | KIT URINE SPECIMEN 50/CA; SYS URINE COLLECTION W/CUP; SYS URINE COLLECTION |
Source: openFDA. Public-domain (CC0).