THUMPER CARDIOPULMONARY RESUSCITATOR

THUMPER CARDIOPULMONARY RESUSCITATOR is an FDA 510(k)-cleared medical device (K962237) manufactured by Michigan Instruments, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 4, 1996. Regulation: 8.