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510(k) Data Aggregation
K Number
K071730Device Name
STUDIODOP VICORDERManufacturer
Date Cleared
2007-12-20
(178 days)
Product Code
Regulation Number
870.2880Type
AbbreviatedPanel
CardiovascularReference & Predicate Devices
N/A
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Device Name :
STUDIODOP VICORDER
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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