
Advanced Bioresearch Assoc.
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DRISTAR URINARY INCONTINENCE MANAGEMENT SYSTEM is an FDA 510(k)-cleared medical device (K950784) manufactured by Advanced Bioresearch Assoc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 2, 1995. Regulation: 8.