THAYER HAND HELD M.K.I. HOLDING CHAMBER

THAYER HAND HELD M.K.I. HOLDING CHAMBER is an FDA 510(k)-cleared medical device (K924535) manufactured by Thayer Medical Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 9, 1993. Regulation: 8.