STANICOR THETA MODEL 221 CARDIAC PACER

STANICOR THETA MODEL 221 CARDIAC PACER is an FDA 510(k)-cleared medical device (K780453) manufactured by Cordis Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on June 29, 1978. Regulation: 8.