
Cardiac Pacemakers, Inc.
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PULSE GENERATOR, BIPOLAR, PROGRAMMABLE is an FDA 510(k)-cleared medical device (K772239) 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 January 29, 1978. Regulation: 8.

ADC
SKU DX606933

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3M Littmann
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