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510(k) Data Aggregation

K Number

Device Name

CRITERION 60 OR PM 60

Manufacturer

Date Cleared

2000-06-22

(90 days)

Product Code

Regulation Number

Type

Panel

Anesthesiology (AN)

Reference & Predicate Devices

N/A

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Device Name :

CRITERION 60 OR PM 60

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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