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510(k) Data Aggregation

K Number

Validate with FDA (Live)

Device Name

BENEVIEW T SERIES PATIENT MONITORS, MODELS BENEVIEW T8, T6 AND T5

Manufacturer

SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD

Date Cleared

2010-08-30

(385 days)

Product Code

Regulation Number

Type

Panel

Age Range

N/A

Reference & Predicate Devices

N/A

Predicate For

K123074,K123211,K132075,K132662,K160981

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

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