TAXI ENDOSCOPIC GUIDEWIRE

TAXI ENDOSCOPIC GUIDEWIRE is an FDA 510(k)-cleared medical device (K081708) manufactured by Lake Region Mfg., 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 August 25, 2008. Regulation: 8.