Scepter Mini Occlusion Balloon Catheter

Scepter Mini Occlusion Balloon Catheter is an FDA 510(k)-cleared medical device (K182829) manufactured by MicroVention, 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 July 9, 2019. Regulation: 8.