FIRSTSAVE BIPHASIC MODEL #9200 AND 9210

FIRSTSAVE BIPHASIC MODEL #9200 AND 9210 is an FDA 510(k)-cleared medical device (K010214) manufactured by Survivalink Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on February 21, 2001. Regulation: 8.