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510(k) Data Aggregation

K Number

Device Name

MANTARAY GUIDEWIRE MODEL M-6000, M-6001, M-6002, M-6003

Manufacturer

BRIDGEPOINT MEDICAL

Date Cleared

2011-06-30

(30 days)

Product Code

Regulation Number

Type

Panel

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N/A

Why did this record match?

Device Name :

MANTARAY GUIDEWIRE MODEL M-6000, M-6001, M-6002, M-6003

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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