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510(k) Data Aggregation
K Number
K955651Device Name
MEDTRONIC SHERPA GUIDING CATHETERManufacturer
Date Cleared
1996-01-22
(41 days)
Product Code
Regulation Number
870.1250Type
TraditionalPanel
Cardiovascular (CV)Reference & Predicate Devices
N/A
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Device Name :
MEDTRONIC SHERPA GUIDING CATHETER
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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