RESPIRONICS BAGEASY ENCOR ADULT SEMI-REUSABLE

RESPIRONICS BAGEASY ENCOR ADULT SEMI-REUSABLE is an FDA 510(k)-cleared medical device (K934699) manufactured by Respironics, 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 January 4, 1995. Regulation: 8.