
Cardiac Pacemakers, Inc.
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SOFTWARE MODULE/2035 PROG AND ASTRA/T PULSE GEN is an FDA 510(k)-cleared medical device (K860584) 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 June 5, 1986. Regulation: 8.

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