Penumbra System Reperfusion Catheter JET 7

Penumbra System Reperfusion Catheter JET 7 is an FDA 510(k)-cleared medical device (K190010) manufactured by Penumbra, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 15, 2019. Regulation: 8.