
Bayer Diagnostics Corp.
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BAYER DIAGNOSTICS ACS:180 AND ADVIA CENTAUR ANTI-TPO ASSAY is an FDA 510(k)-cleared medical device (K003291) manufactured by Bayer Diagnostics Corp.. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 4, 2000. Regulation: 8.