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510(k) Data Aggregation

K Number

Device Name

N-ASSAY TIA FIBRINOGEN TEST KIT

Manufacturer

CRESTAT DIAGNOSTICS, INC.

Date Cleared

1997-04-16

(117 days)

Product Code

Regulation Number

Type

Panel

Reference & Predicate Devices

N/A

Why did this record match?

Device Name :

N-ASSAY TIA FIBRINOGEN TEST KIT

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

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AI/ML Overview

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