
Columbia Bioscience, Inc.
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IS-ANTI-MPO IGG ELISA TEST SYSTEM is an FDA 510(k)-cleared medical device (K983390) manufactured by Columbia Bioscience, Inc.. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 17, 1998. Regulation: 8.