FDA Device Establishments · JSON-LD · Markdown
FEI 3030003849 · Manufacture Medical Device · Status: Active
| FEI Number | 3030003849 |
|---|---|
| Owner / Operator | Nuvascular Inc. (#10091454) |
| Address | 141 Innovation Dr Ste 100, Irvine, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KRD |
| Regulation § (21 CFR) | 870.3300 |
| Proprietary names | HARBOR Occlusion Device |
Source: openFDA. Public-domain (CC0).