FILTER, AIR, CUTTER MAINLINE

FILTER, AIR, CUTTER MAINLINE is an FDA 510(k)-cleared medical device (K770375) manufactured by Cutter Laboratories, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 28, 1977. Regulation: 8.