Penumbra, Inc. - FDA 510(k) Cleared Devices
Recent clearances: INDIGO® Aspiration System – INDIGO Link, INDIGO® Aspiration System - Lightning Flash Aspiration Tubing with LINK, INDIGO® Aspiration System – Lightning Flash Aspiration Tubing
86
Total
84
Cleared
0
Denied
FDA 510(k) Regulatory Record - Penumbra, Inc. Physical Medicine ✕
1 devices