AngioSafe
Matched from indexed company URL: AngioSafe, Inc.
FDA Registration(s)#
Registration, FEI, Name table| Registration | FEI | Name | Status | Initial importer | Expiration year | Address |
|---|
| 3013757884 | 3013757884 | AngioSafe | 1 | N | 2026-01-01 | 5215 Hellyer Ave Ste 240 San Jose CA US 95138 |
| 3013757884 | 3013757884 | ANGIOSAFE | 1 | N | 2020-04-25 | 6150 Hellyer Avenue Suite 150 San Jose CA US 95138 |
Registered Device Listings#
Registration key, Listing key, Premarket submission table| Registration key | Listing key | Premarket submission | Device | Product code | Decision date |
|---|
| 336706 | 2063788779 | K252315 | Santreva™-ATK Endovascular Revasculariztion Catheter | PDU | 2025-09-22 |
| 209877 | 2038976038 | | | | |
Product Codes Associated With Registrations#
Product code, Registration listing records, Latest decision table| Product code | Registration listing records | Latest decision |
|---|
| PDU | 1 | 2025-09-22 |
PMN#
2025-09-22
AngioSafe, Inc.
GUDID#
Angiosafe, Inc.
2025-12-03