VICKERS MEDICAL MODEL 130 NEAVENT-NEO

VICKERS MEDICAL MODEL 130 NEAVENT-NEO is an FDA 510(k)-cleared medical device (K791713) manufactured by Vickers America 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 September 18, 1979. Regulation: 8.