Bip USA, Inc.
BIP BIOPSY NEEDLE MODIFICATION
SKU K934370UPC FCG
In Stock
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IIFDA 510(k) Cleared (K934370)
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Free shipping on orders over $99 · 30-day returns
Bip USA, Inc.
Free shipping on orders over $99 · 30-day returns
BIP BIOPSY NEEDLE MODIFICATION is an FDA 510(k)-cleared medical device (K934370) manufactured by Bip USA, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 6, 1994. Regulation: 8.
