PANAMEX(TM) URETERAL STENT

PANAMEX(TM) URETERAL STENT is an FDA 510(k)-cleared medical device (K882157) manufactured by Kingston Technologies, 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 August 1, 1988. Regulation: 8.