MODIFICATION TO MALE TO MALE LUER ADAPTER

MODIFICATION TO MALE TO MALE LUER ADAPTER is an FDA 510(k)-cleared medical device (K003712) manufactured by Molded Products, 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 May 15, 2001. Regulation: 8.