
The DU Pont Co.
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ACA THYRONINE UPTAKE (TU E) METHOD is an FDA 510(k)-cleared medical device (K885259) manufactured by The DU Pont Co.. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 16, 1989. Regulation: 8.