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510(k) Data Aggregation
K Number
K000210Manufacturer
Date Cleared
2000-02-23
(30 days)
Product Code
Regulation Number
870.3620Type
SpecialPanel
CardiovascularReference & Predicate Devices
N/A
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Device Name :
MODIFICATION TO MODEL 5866-37M LEAD ADAPTOR KIT
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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