PULMONARY RESUSCITATOR, MODIFICATION

PULMONARY RESUSCITATOR, MODIFICATION is an FDA 510(k)-cleared medical device (K892221) manufactured by Life Design Systems, 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 17, 1989. Regulation: 8.