MODEL 20 DIGITAL PULSE RATE MONITOR

MODEL 20 DIGITAL PULSE RATE MONITOR is an FDA 510(k)-cleared medical device (K780937) manufactured by Sentronix, 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 August 30, 1978. Regulation: 8.