FDA Device Establishments · JSON-LD · Markdown
FEI 3006602209 · Manufacture Medical Device · Status: Active
| FEI Number | 3006602209 |
|---|---|
| Owner / Operator | Lumos Diagnostics, Inc. (#9075965) |
| Address | 2724 Loker Avenue, Carlsbad, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | QXA |
| Regulation § (21 CFR) | 866.3230 |
| Proprietary names | FebriDx Bacterial / Non-Bacterial Assay; INDICAID FebriDx Bacterial / Non-Bacterial Assay |
Source: openFDA. Public-domain (CC0).