ATTENDS INCONTINENT BRIEF

ATTENDS INCONTINENT BRIEF is an FDA 510(k)-cleared medical device (K873036) manufactured by Procter & Gamble Mfg. Co.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 18, 1988. Regulation: 8.