ASTRA T2, T3, T4, T6 PULSE GENERATORS NEW PACKAGE

ASTRA T2, T3, T4, T6 PULSE GENERATORS NEW PACKAGE is an FDA 510(k)-cleared medical device (K890785) manufactured by Cardiac Pacemakers, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on March 9, 1989. Regulation: 8.