
Bayer Corp.
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BAYER ADVIA IMS SYSTEM (IN VITRO DIAGNOSTIC SYSTEM) is an FDA 510(k)-cleared medical device (K982328) manufactured by Bayer 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 January 28, 1999. Regulation: 8.