FDA Device Establishments · JSON-LD · Markdown
FEI 3009964638 · Remanufacture Medical Device Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active
| FEI Number | 3009964638 |
|---|---|
| Owner / Operator | AccuVein, Inc. (#10026504) |
| Address | 848 Gish Road, Suite 5, San Jose, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KZA |
| Regulation § (21 CFR) | 880.6970 |
| Proprietary names | AV600; AV300; AccuVein HF550 Hands-Free Stand; HF580 Hands-Free Powered Goose Neck Wheeled Stand; AccuVein HF510 Hands-Free Stand; AV500; AV400 |
Source: openFDA. Public-domain (CC0).