Angioscore, Inc.
ANGIOSCULPT PTA SCORING BALLOON CATHETER, MODELS 2076-6040, 2092-6040, 2105-6040
SKU K091966UPC PNO
In Stock
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IIFDA 510(k) Cleared (K091966)
1
Free shipping on orders over $99 · 30-day returns
Angioscore, Inc.
Free shipping on orders over $99 · 30-day returns
ANGIOSCULPT PTA SCORING BALLOON CATHETER, MODELS 2076-6040, 2092-6040, 2105-6040 is an FDA 510(k)-cleared medical device (K091966) 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 July 29, 2009. Regulation: 8.
