SENTINEL RECORDER, MODELS 471/472

SENTINEL RECORDER, MODELS 471/472 is an FDA 510(k)-cleared medical device (K971696) manufactured by Del Mar Avionics. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 29, 1997. Regulation: 8.