K.P.R. (KING PERSONAL RESUSCITATOR)

K.P.R. (KING PERSONAL RESUSCITATOR) is an FDA 510(k)-cleared medical device (K943402) manufactured by King Systems Corp.. 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 18, 1994. Regulation: 8.