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FDA 510(k) Applications for Medical Device Product Code "OQZ"
(Anti-Mutated Citrullinated Vimentin Igg)
FDA 510(k) Number
Applicant
Device Name
Decision Date
K092399
ORGENTEC DIAGNOSTIKA GMBH
ANTI-MUTATED CITRULLINATED VIMENTIN EIA
07/01/2010
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