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510(k) Data Aggregation
K Number
K010004Manufacturer
Date Cleared
2001-02-13
(42 days)
Product Code
Regulation Number
870.1210Type
SpecialPanel
CardiovascularReference & Predicate Devices
N/A
Why did this record match?
Device Name :
FLOWRIDER FLOW DIRECTED MICRO CATHETER, MODEL 105-5065
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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