
King Diagnostics, Inc.
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KD ACTIVATED PARTIAL THROMBOPLASTIN TIME REAGENT is an FDA 510(k)-cleared medical device (K884485) manufactured by King Diagnostics, 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 December 27, 1988. Regulation: 8.