SIMS 1ST RESPONSE MANUAL RESUSCITATOR, ADULT

SIMS 1ST RESPONSE MANUAL RESUSCITATOR, ADULT is an FDA 510(k)-cleared medical device (K972283) manufactured by Sims. 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 16, 1997. Regulation: 8.