MCKERNAN ATRAUMATIC FORCEPS

MCKERNAN ATRAUMATIC FORCEPS is an FDA 510(k)-cleared medical device (K925041) manufactured by Aslan Medical Technologies, Ltd.. 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 November 24, 1992. Regulation: 8.