FDA Device Establishments · JSON-LD · Markdown
FEI 3032277090 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3032277090 |
|---|---|
| Owner / Operator | Vantis Vascular, Inc. (#10091990) |
| Address | 2570 N 1st St Ste 200, San Jose, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | DQY |
| Regulation § (21 CFR) | 870.1250 |
| Proprietary names | CrossFAST Integrated Microcatheter Advanced Delivery System; CrossFAST Integrated Microcatheter Guide Extension System |
Source: openFDA. Public-domain (CC0).