LIFEPAK 5 CARDIOSCOPE-RECORDER MODULE

LIFEPAK 5 CARDIOSCOPE-RECORDER MODULE is an FDA 510(k)-cleared medical device (K760676) manufactured by Physio-Control Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 12, 1976. Regulation: 8.