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510(k) Data Aggregation
K Number
K241963Device Name
WERAYManufacturer
Date Cleared
2024-07-30
(27 days)
Product Code
Regulation Number
872.1800Type
TraditionalPanel
Radiology (RA)Reference & Predicate Devices
N/A
Why did this record match?
Device Name :
WERAY
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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