STILITH CARDIAC PACEMAKERS-M. 60 & 120

STILITH CARDIAC PACEMAKERS-M. 60 & 120 is an FDA 510(k)-cleared medical device (K780781) manufactured by R.E. Brown Co., Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on July 26, 1978. Regulation: 8.