RETROX RX 45-JBP 124774, 53-JBP 124775, 53-BP 124776, 60-124777

RETROX RX 45-JBP 124774, 53-JBP 124775, 53-BP 124776, 60-124777 is an FDA 510(k)-cleared medical device (K990483) manufactured by Biotronik, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on June 2, 1999. Regulation: 8.