PROGRAMALITH III-3 MODEL 231 PULSE GENERATOR

PROGRAMALITH III-3 MODEL 231 PULSE GENERATOR is an FDA 510(k)-cleared medical device (K850651) manufactured by Pacesetter Systems. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on March 31, 1985. Regulation: 8.