DIALOG MODELS 748, 748K AND 748T PULSE GENERATORS

DIALOG MODELS 748, 748K AND 748T PULSE GENERATORS is an FDA 510(k)-cleared medical device (K862226) 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 February 2, 1987. Regulation: 8.