URETEROPYELOGRAM CATH FOR RETROGRADE DYE INJECTION

URETEROPYELOGRAM CATH FOR RETROGRADE DYE INJECTION is an FDA 510(k)-cleared medical device (K903994) manufactured by Applied Urology, Inc.. 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 18, 1990. Regulation: 8.