
Aqua-Med Systems, Inc.
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SERVICE DEIONIZATION SYST/DI TANK EXCHANGE PROGRAM is an FDA 510(k)-cleared medical device (K915258) manufactured by Aqua-Med Systems, 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 July 1, 1993. Regulation: 8.