RESPIRATION/8100-HEART RATE RECORDER

RESPIRATION/8100-HEART RATE RECORDER is an FDA 510(k)-cleared medical device (K833348) manufactured by Aequitron Medical, 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 April 16, 1984. Regulation: 8.