Penumbra, Inc.
PENUMBRA BALLOON GUIDE CATHETER, MODEL 7.5F
SKU K053491UPC DQY
In Stock
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IIFDA 510(k) Cleared (K053491)
1
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Penumbra, Inc.
Free shipping on orders over $99 · 30-day returns
PENUMBRA BALLOON GUIDE CATHETER, MODEL 7.5F is an FDA 510(k)-cleared medical device (K053491) manufactured by Penumbra, 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 April 26, 2006. Regulation: 8.
