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510(k) Data Aggregation
K Number
K052473Manufacturer
Date Cleared
2005-10-28
(49 days)
Product Code
Regulation Number
892.1100Type
TraditionalPanel
RadiologyReference & Predicate Devices
N/A
Why did this record match?
Device Name :
CX 250 C PLUS WITH GAMMAXP SOFTWARE, MODEL 0121 0000
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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