VANGUARD REPROCESSED ENDOSCOPIC INSTRUMENTS

VANGUARD REPROCESSED ENDOSCOPIC INSTRUMENTS is an FDA 510(k)-cleared medical device (K012700) manufactured by Vanguard Medical Concepts, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 6, 2001. Regulation: 8.