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510(k) Data Aggregation
K Number
K000159Manufacturer
Date Cleared
2000-02-16
(28 days)
Product Code
Regulation Number
892.1630Type
SpecialPanel
RadiologyReference & Predicate Devices
N/A
Why did this record match?
Device Name :
AGFA DIAGNOSTIC CENTER ADC, ADC COMPACT, AND ADC SOLO
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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