United States Endoscopy Group, Inc.
LAPAROSCOPIC LASER FIBER DIVERTER
SKU K912502UPC GCJ
In Stock
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IIFDA 510(k) Cleared (K912502)
1
Free shipping on orders over $99 · 30-day returns
United States Endoscopy Group, Inc.
Free shipping on orders over $99 · 30-day returns
LAPAROSCOPIC LASER FIBER DIVERTER is an FDA 510(k)-cleared medical device (K912502) 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 July 24, 1991. Regulation: 8.
