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510(k) Data Aggregation
K Number
K000632Device Name
0.9% SODIUM CHLORIDE VASCULAT ACCESS DEVICEManufacturer
Date Cleared
2000-10-19
(238 days)
Product Code
Regulation Number
880.5200Type
TraditionalPanel
General HospitalReference & Predicate Devices
N/A
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Device Name :
0.9% SODIUM CHLORIDE VASCULAT ACCESS DEVICE
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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