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510(k) Data Aggregation

K Number

Device Name

PATHWAY ELECTROMYOGRAPH MODEL PATHWAY II/MR-10/MR-15/MR-20/MR-25

Manufacturer

THE PROMETHEUS GROUP

Date Cleared

1997-01-16

(346 days)

Product Code

Regulation Number

Type

Panel

Gastroenterology/Urology

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N/A

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Device Name :

PATHWAY ELECTROMYOGRAPH MODEL PATHWAY II/MR-10/MR-15/MR-20/MR-25

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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