VASCOSCREW 6/60 AND VASCOSCREW 8/60

VASCOSCREW 6/60 AND VASCOSCREW 8/60 is an FDA 510(k)-cleared medical device (K914121) manufactured by Vascor Medical Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on August 23, 1993. Regulation: 8.