FDA Device Establishments · JSON-LD · Markdown
FEI 3013757884 · Manufacture Medical Device · Status: Active
| FEI Number | 3013757884 |
|---|---|
| Owner / Operator | AngioSafe (#10055439) |
| Address | 5215 Hellyer Ave Ste 240, San Jose, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | PDU |
| Regulation § (21 CFR) | 870.1250 |
| Proprietary names | Santreva-ATK Endovascular Revascularization Catheter |
Source: openFDA. Public-domain (CC0).