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510(k) Data Aggregation
K Number
K003533Device Name
CROSS-CHECKS LF, MODEL CI 119/S &CI 119/LManufacturer
Date Cleared
2001-02-07
(83 days)
Product Code
Regulation Number
880.2800Type
AbbreviatedPanel
General HospitalReference & Predicate Devices
N/A
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Device Name :
CROSS-CHECKS LF, MODEL CI 119/S &CI 119/L
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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