B.A.S.E. BELLOWS AIR SUPPORT EQUIPMENT

B.A.S.E. BELLOWS AIR SUPPORT EQUIPMENT is an FDA 510(k)-cleared medical device (K915671) manufactured by Progressive Medical Technology, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 12, 1992. Regulation: 8.