
Millipore Corp.
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FILTER, PERITONEAL DIALY. ADMIN. SET is an FDA 510(k)-cleared medical device (K772236) manufactured by Millipore Corp.. 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 January 23, 1978. Regulation: 8.