FDA Device Establishments · JSON-LD · Markdown
FEI 3013505221 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3013505221 |
|---|---|
| Owner / Operator | ABK Biomedical (#10086030) |
| Address | 155 Chain Lake Drive, Unit 32, Halifax Nova Scotia, B3S 1B3, CA |
| Mandatory US Agent | ABK Biomedical, Inc |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KRD |
| Regulation § (21 CFR) | 870.3300 |
| Proprietary names | Easi-Vue® embolic microspheres System |
Source: openFDA. Public-domain (CC0).