CATHETER, DISP., EXTERNAL, MALE

CATHETER, DISP., EXTERNAL, MALE is an FDA 510(k)-cleared medical device (K772144) manufactured by Medline Industries, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 27, 1977. Regulation: 8.