PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV

PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV is an FDA 510(k)-cleared medical device (K890182) manufactured by Aesculap Instruments Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 27, 1990. Regulation: 8.