Penumbra, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Penumbra System (Thunderbolt Aspiration Tubing), INDIGO® Aspiration System – INDIGO Link, INDIGO® Aspiration System - Lightning Flash Aspiration Tubing with LINK
87
Total
85
Cleared
0
Denied
FDA 510(k) Regulatory Record - Penumbra, Inc. General & Plastic Surgery ✕
2 devices