PULSE GENERATOR 698, 698B & 698L

PULSE GENERATOR 698, 698B & 698L is an FDA 510(k)-cleared medical device (K841229) 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 June 24, 1984. Regulation: 8.