Biopsys Medical, Inc.
MODIFIED BIOPSY NEEDLE
SKU K951229UPC KNW
In Stock
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IIFDA 510(k) Cleared (K951229)
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Free shipping on orders over $99 · 30-day returns
Biopsys Medical, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFIED BIOPSY NEEDLE is an FDA 510(k)-cleared medical device (K951229) manufactured by Biopsys Medical, 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 April 5, 1995. Regulation: 8.
