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510(k) Data Aggregation

K Number

Device Name

REMEL STAPH LATEX KIT

Manufacturer

Date Cleared

1997-02-07

(101 days)

Product Code

Regulation Number

Type

Panel

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N/A

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Device Name :

REMEL STAPH LATEX KIT

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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