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510(k) Data Aggregation
K Number
K240246Manufacturer
Date Cleared
2024-07-26
(178 days)
Product Code
Regulation Number
870.1390Type
TraditionalPanel
CardiovascularReference & Predicate Devices
N/A
Why did this record match?
Device Name :
Accusafe Transseptal Guidewire (GTR31180, GTR31230)
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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