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510(k) Data Aggregation
K Number
K960309Manufacturer
Date Cleared
1997-02-28
(420 days)
Product Code
Regulation Number
868.5440Type
TraditionalPanel
AnesthesiologyReference & Predicate Devices
N/A
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Device Name :
AIRSEP NEWLIFE DUAL SIX OXYGEN CONCENTRATOR (MODIFICATION)
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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