BAHO AUTOCLAVABLE CYSTOSCOPE

BAHO AUTOCLAVABLE CYSTOSCOPE is an FDA 510(k)-cleared medical device (K992983) manufactured by Innovative Endoscopy Components, LLC. 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 6, 1999. Regulation: 8.