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510(k) Data Aggregation
K Number
K960216Device Name
CPR SUCTION CATHETER KITManufacturer
Date Cleared
1996-04-15
(90 days)
Product Code
Regulation Number
880.6740Type
TraditionalPanel
General HospitalReference & Predicate Devices
N/A
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Device Name :
CPR SUCTION CATHETER KIT
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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