ASTRA 2, ASTRA 3, 4 & 6

ASTRA 2, ASTRA 3, 4 & 6 is an FDA 510(k)-cleared medical device (K842394) 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 16, 1984. Regulation: 8.