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510(k) Data Aggregation
K Number
K000209Device Name
DOSE 1Manufacturer
Date Cleared
2000-08-18
(207 days)
Product Code
Regulation Number
892.5050Type
TraditionalPanel
RadiologyReference & Predicate Devices
N/A
Why did this record match?
Applicant Name (Manufacturer) :
SCANDITRONIX WELLHOFER NORTH AMERICA
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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