MODEL 255A PROGRAMMER III, W/SOFTWARE REVI. 4004

MODEL 255A PROGRAMMER III, W/SOFTWARE REVI. 4004 is an FDA 510(k)-cleared medical device (K882429) manufactured by Tpl-Cordis, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on July 21, 1988. Regulation: 8.