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510(k) Data Aggregation
K Number
K004007Device Name
DR180+OXYManufacturer
Date Cleared
2001-01-25
(30 days)
Product Code
Regulation Number
870.2800Type
SpecialPanel
CardiovascularReference & Predicate Devices
N/A
Why did this record match?
Device Name :
DR180+OXY
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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