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510(k) Data Aggregation

K Number

Device Name

ACCESS VITAMIN B12 ASSAY (MODIFICATION)

Manufacturer

BIO-RAD LABORATORIES, INC.

Date Cleared

1996-01-24

(114 days)

Product Code

Regulation Number

Type

Panel

Clinical Chemistry

Reference & Predicate Devices

N/A

Why did this record match?

Device Name :

ACCESS VITAMIN B12 ASSAY (MODIFICATION)

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

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