PRIMA 236-02 NONPROGRAMMABLE CARDIAC

PRIMA 236-02 NONPROGRAMMABLE CARDIAC is an FDA 510(k)-cleared medical device (K841404) manufactured by Intermedics, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on May 29, 1984. Regulation: 8.