
Endothelix, Inc.
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VENDYS, MODEL 6000 B B/C is an FDA 510(k)-cleared medical device (K072919) manufactured by Endothelix, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 1, 2007. Regulation: 8.