Angioscore, Inc.
ANGIOSCULPT SCORING BALLOON CATHETER
SKU K050629UPC PNO
In Stock
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IIFDA 510(k) Cleared (K050629)
1
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Angioscore, Inc.
Free shipping on orders over $99 · 30-day returns
ANGIOSCULPT SCORING BALLOON CATHETER is an FDA 510(k)-cleared medical device (K050629) 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 September 1, 2005. Regulation: 8.
