PULSE GENERATOR 696, 696B & 696L

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.