AFP CARDIAC PACING SYSTEM MODEL 283 (MODIFICATION)

AFP CARDIAC PACING SYSTEM MODEL 283 (MODIFICATION) is an FDA 510(k)-cleared medical device (K954714) manufactured by Pacesetter, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on January 31, 1996. Regulation: 8.