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510(k) Data Aggregation
K Number
K003444Manufacturer
Date Cleared
2000-11-21
(15 days)
Product Code
Regulation Number
870.1130Type
TraditionalPanel
CardiovascularReference & Predicate Devices
N/A
Why did this record match?
Device Name :
MODEL WS-500 DIGITAL WRIST BLOOD PRESSURE MONITOR
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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