
Roche Diagnostics Corp.
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MODIFICATION TO CALIBRATOR FOR AUTOMATIC SYSTEMS (CFAS) is an FDA 510(k)-cleared medical device (K033501) manufactured by Roche Diagnostics Corp.. 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 November 19, 2003. Regulation: 8.