KSEA QUADRO SWITCH

KSEA QUADRO SWITCH is an FDA 510(k)-cleared medical device (K021776) manufactured by Karl Storz Endoscopy. 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 14, 2002. Regulation: 8.