1ST RESPONSE (TM) INFANT MANUAL RESUSCITATOR

1ST RESPONSE (TM) INFANT MANUAL RESUSCITATOR is an FDA 510(k)-cleared medical device (K902733) manufactured by Intertech Resources, 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 August 21, 1990. Regulation: 8.