FDA Device Establishments · JSON-LD · Markdown
FEI 3039062605 · Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3039062605 |
|---|---|
| Owner / Operator | Corvitex Corporation (#10092281) |
| Address | 4928 Windy Hill Dr Ste B, Raleigh, NC, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | DQY |
| Regulation § (21 CFR) | 870.1250 |
| Proprietary names | Primum Guiding Catheter |
Source: openFDA. Public-domain (CC0).