ACKRAD V/CUG VOIDING CYSTOURETHROGRAPHY SET

ACKRAD V/CUG VOIDING CYSTOURETHROGRAPHY SET is an FDA 510(k)-cleared medical device (K874293) manufactured by Ackrad Laboratories. 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 December 28, 1987. Regulation: 8.