FDA Device Establishments · JSON-LD · Markdown
FEI 3002808498 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3002808498 |
|---|---|
| Owner / Operator | Revvity, Inc. (#9912035) |
| Address | MUSTIONKATU 6, TURKU Varsinais-Suomi, 20750, FI |
| Mandatory US Agent | Revvity, Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | LOK |
| Proprietary names | AutoDELFIA hAFP kit (B079-212); AutoDELFIA instrument |
Source: openFDA. Public-domain (CC0).