Popper & Sons, Inc.
WESTERMAN-JENSEN BIOPSY NEEDLE
SKU K840168UPC FCG
In Stock
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IIFDA 510(k) Cleared (K840168)
1
Free shipping on orders over $99 · 30-day returns
Popper & Sons, Inc.
Free shipping on orders over $99 · 30-day returns
WESTERMAN-JENSEN BIOPSY NEEDLE is an FDA 510(k)-cleared medical device (K840168) manufactured by Popper & Sons, 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 11, 1984. Regulation: 8.
