Cardiosolutions, Inc.
PERCU-PRO GUIDEWIRE
SKU K094062UPC DQX
In Stock
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IIFDA 510(k) Cleared (K094062)
1
Free shipping on orders over $99 · 30-day returns
Cardiosolutions, Inc.
Free shipping on orders over $99 · 30-day returns
PERCU-PRO GUIDEWIRE is an FDA 510(k)-cleared medical device (K094062) manufactured by Cardiosolutions, 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 26, 2010. Regulation: 8.
