Name: MODIFICATION TO ANGIOSCULPT PTA SCORING BALLOON CATHETER
Brand: Angioscore, Inc.
SKU: K081220

MODIFICATION TO ANGIOSCULPT PTA SCORING BALLOON CATHETER is an FDA 510(k)-cleared medical device (K081220) manufactured by Angioscore, 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 May 27, 2008. Regulation: 8.

MODIFICATION TO ANGIOSCULPT PTA SCORING BALLOON CATHETER

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