
H.W. Andersen Products, Inc.
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AN3200 DOUBILET DRAIN is an FDA 510(k)-cleared medical device (K872458) manufactured by H.W. Andersen 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 September 20, 1987. Regulation: 8.