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510(k) Data Aggregation
K Number
K001439Device Name
ORTHOCEPH OC100 DManufacturer
Date Cleared
2000-06-22
(45 days)
Product Code
Regulation Number
872.1800Type
TraditionalPanel
RadiologyReference & Predicate Devices
N/A
Why did this record match?
Device Name :
ORTHOCEPH OC100 D
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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