
Olympus America, Inc.
Free shipping on orders over $99 · 30-day returns
OLYMPUS KD-6G1-9Q WIRE GUIDED PAPILLOTOMU KNIFE is an FDA 510(k)-cleared medical device (K950166) manufactured by Olympus America, 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 February 21, 1995. Regulation: 8.