
Chiron Diagnostics Corp.
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CHIRON DIAGNOSTICS ACS: 180 FERRITIN ASSAY is an FDA 510(k)-cleared medical device (K992157) manufactured by Chiron 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 August 4, 1999. Regulation: 8.