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510(k) Data Aggregation

K Number

Device Name

ARIETTA 60/ARIETTAS60/ARIETTAV60

Manufacturer

HITACHI ALOKA MEDICAL,LTD. (HITACHI ALOKA MEDICAL

Date Cleared

2014-06-16

(115 days)

Product Code

Regulation Number

Type

Panel

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N/A

Why did this record match?

Device Name :

ARIETTA 60/ARIETTAS60/ARIETTAV60

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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