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510(k) Data Aggregation
K Number
K002237Device Name
P3IMRT TMManufacturer
Date Cleared
2001-02-02
(193 days)
Product Code
Regulation Number
892.5050Type
TraditionalPanel
RadiologyReference & Predicate Devices
N/A
Why did this record match?
Device Name :
P3IMRT TM
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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