
Siemens Elema AB
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PULSE GENERATOR 696, 696B & 696L is an FDA 510(k)-cleared medical device (K841232) manufactured by Siemens Elema AB. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on December 2, 1984. Regulation: 8.

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