United States Endoscopy Group, Inc.
NEEDLE
SKU K924102UPC FBK
In Stock
—
IIFDA 510(k) Cleared (K924102)
1
Free shipping on orders over $99 · 30-day returns
United States Endoscopy Group, Inc.
Free shipping on orders over $99 · 30-day returns
NEEDLE is an FDA 510(k)-cleared medical device (K924102) manufactured by United States Endoscopy Group, 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 November 24, 1992. Regulation: 8.
