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510(k) Data Aggregation
K Number
K950613Device Name
KEISEIManufacturer
Date Cleared
1996-02-14
(369 days)
Product Code
Regulation Number
868.5110Type
TraditionalPanel
AnesthesiologyReference & Predicate Devices
N/A
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Applicant Name (Manufacturer) :
KEISEI (USA) CO., LTD.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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