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510(k) Data Aggregation
K Number
K010767Manufacturer
Date Cleared
2001-04-10
(27 days)
Product Code
Regulation Number
880.5965Type
SpecialPanel
Hematology (HO)Reference & Predicate Devices
N/A
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Device Name :
LIFEPORT VTX ACCESS SYSTEM,MODEL VTX 7000 SERIES
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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