United States Endoscopy Group, Inc.
U.S. ENDOSCOPY GROUP, INC. BALLOON REPLACEMENT GASTROSTOMY TUBE
SKU K955181UPC KNT
In Stock
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IIFDA 510(k) Cleared (K955181)
1
Free shipping on orders over $99 · 30-day returns
United States Endoscopy Group, Inc.
Free shipping on orders over $99 · 30-day returns
U.S. ENDOSCOPY GROUP, INC. BALLOON REPLACEMENT GASTROSTOMY TUBE is an FDA 510(k)-cleared medical device (K955181) 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 June 4, 1996. Regulation: 8.
