MODIFIED MODELS 9500,9550,9200,8200,HEART RATE MON

MODIFIED MODELS 9500,9550,9200,8200,HEART RATE MON is an FDA 510(k)-cleared medical device (K902785) manufactured by Aequitron Medical, 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 July 12, 1990. Regulation: 8.