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510(k) Data Aggregation
K Number
K123152Device Name
VITESSE 3.0Manufacturer
Date Cleared
2012-12-07
(59 days)
Product Code
Regulation Number
892.5050Type
TraditionalPanel
RadiologyReference & Predicate Devices
N/A
Why did this record match?
Device Name :
VITESSE 3.0
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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