PLUS REUSABLE RESUSCITATOR

PLUS REUSABLE RESUSCITATOR is an FDA 510(k)-cleared medical device (K974141) manufactured by Schiff & Co.. 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 20, 1998. Regulation: 8.