FDA Device Establishments · JSON-LD · Markdown
FEI 3005984081 · Repack or Relabel Medical Device · Status: Active
| FEI Number | 3005984081 |
|---|---|
| Owner / Operator | LUMIQUICK DIAGNOSTICS, INC. (#9093981) |
| Address | 2946 SCOTT BLVD., SANTA CLARA, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | CEP |
| Regulation § (21 CFR) | 862.1485 |
Source: openFDA. Public-domain (CC0).