
Organon, Inc.
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OREIA-Q-TY, ENZYME IMMUNOASSAY is an FDA 510(k)-cleared medical device (K802693) manufactured by Organon, Inc.. 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 December 9, 1980. Regulation: 8.