Medical Device Manufacturer · US , Redwood City , CA

Intervene - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2025

1

Total

1

Cleared

0

Denied

FDA 510(k) cleared devices by Intervene Cardiovascular ✕

1 devices

1-1 of 1

Cleared Oct 22, 2025

Recana Thrombectomy Catheter System (FG014. FG015, FG016, FG017, FG018,...

Cardiovascular · 189d