Indigo Aspiration System - Modified 110 Aspiration Tubing

Indigo Aspiration System - Modified 110 Aspiration Tubing is an FDA 510(k)-cleared medical device (K180939) 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 May 2, 2018. Regulation: 8.