ASTRA T2, ASTRA T4, ASTRA T6

ASTRA T2, ASTRA T4, ASTRA T6 is an FDA 510(k)-cleared medical device (K920601) 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 October 27, 1992. Regulation: 8.