MAXIM PF MODELS 033-581/033-590

MAXIM PF MODELS 033-581/033-590 is an FDA 510(k)-cleared medical device (K961118) manufactured by Telectronics Pacing Systems, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on July 14, 1996. Regulation: 8.