FDA Device Establishments · JSON-LD · Markdown
FEI 3007145015 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3007145015 |
|---|---|
| Owner / Operator | Revvity, Inc. (#9912035) |
| Address | 17 P&N Drive, Greenville, SC, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | PJC |
| Regulation § (21 CFR) | 862.1675 |
| Proprietary names | Revvity 226 Sample Collection Device; Contract Manufactured Collection Device with Ahlstrom 226 filter paper. |
Source: openFDA. Public-domain (CC0).