BAGEASY(R) III CHILD/INFANT DISPOS MAN RESUSCITATORS

BAGEASY(R) III CHILD/INFANT DISPOS MAN RESUSCITATORS is an FDA 510(k)-cleared medical device (K940581) 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 May 5, 1994. Regulation: 8.