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510(k) Data Aggregation
K Number
K960466Manufacturer
Date Cleared
1996-05-29
(148 days)
Product Code
Regulation Number
880.5440Type
TraditionalPanel
General HospitalReference & Predicate Devices
N/A
Why did this record match?
Device Name :
IVEX-2 EXTENSION SET WITH Y-INJECTION SITE (MODIFICATION)
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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