
Diatech, Inc.
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DIA T1, T2 & T3 is an FDA 510(k)-cleared medical device (K842286) manufactured by Diatech, Inc.. This device is classified under the Hematology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 10, 1984. Regulation: 8.