CIRCON ACMI BICAP HEMORRHOID SYSTEM BH-10 & BHP-20

CIRCON ACMI BICAP HEMORRHOID SYSTEM BH-10 & BHP-20 is an FDA 510(k)-cleared medical device (K884252) manufactured by Circon Acmi. 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 January 9, 1989. Regulation: 8.