SKINNY,FRANSEEN,WESCOTT NEEDLES

SKINNY,FRANSEEN,WESCOTT NEEDLES is an FDA 510(k)-cleared medical device (K962907) manufactured by Baxter Healthcare Corp. 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 October 22, 1996. Regulation: 8.