FDA 510(k), K110641, FUJIREBIO DIAGNOSTICS VITAMIN D CONTROL
FDA 510(k), K110641, FUJIREBIO DIAGNOSTICS VITAMIN D CONTROL
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510(K) Number: K110641
Device Name: FUJIREBIO DIAGNOSTICS VITAMIN D CONTROL
Manufacturer:
Device Classification Name: Single (Specified) Analyte Controls (Assayed And Unassayed)
Regulation Number: 862.1660
Classification Product Code: JJX
Date Received: 03/04/2011
Decision Date: 05/27/2011
Regulation Medical Specialty: Clinical Chemistry
Device Name: FUJIREBIO DIAGNOSTICS VITAMIN D CONTROL
Manufacturer:
Device Classification Name: Single (Specified) Analyte Controls (Assayed And Unassayed)
Regulation Number: 862.1660
Classification Product Code: JJX
Date Received: 03/04/2011
Decision Date: 05/27/2011
Regulation Medical Specialty: Clinical Chemistry