MATRX HOPE(R) 5 RESUSCITATOR

MATRX HOPE(R) 5 RESUSCITATOR is an FDA 510(k)-cleared medical device (K921982) manufactured by Matrix Medica, 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 October 27, 1994. Regulation: 8.