INTERVENE INC
FDA Registration(s)#
| Registration | FEI | Name | Status | Initial importer | Expiration year | Address |
|---|---|---|---|---|---|---|
| 3030481118 | 3030481118 | INTERVENE INC | 1 | N | 2026-01-01 | 2684 Middlefield Rd Ste E Redwood City CA US 94063 |
Registered Device Listings#
| Registration key | Listing key | Premarket submission | Device | Product code | Decision date |
|---|---|---|---|---|---|
| 344188 | 1593023701 | K251185 | Recana Thrombectomy Catheter System (FG014. FG015, FG016, FG017, FG018, FG019, FG020) | QEW | 2025-10-22 |
Product Codes Associated With Registrations#
| Product code | Registration listing records | Latest decision |
|---|---|---|
| QEW | 1 | 2025-10-22 |