PULSE GENERATOR 728, 728B & 728L

PULSE GENERATOR 728, 728B & 728L is an FDA 510(k)-cleared medical device (K841226) 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 25, 1984. Regulation: 8.