TRIOS-M VS-1 PULSE GENERATOR

TRIOS-M VS-1 PULSE GENERATOR is an FDA 510(k)-cleared medical device (K863878) manufactured by Biotronik Sales, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on December 9, 1986. Regulation: 8.