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510(k) Data Aggregation
K Number
K952910Device Name
THE SWIRLER NEBULIZERManufacturer
Date Cleared
1997-03-19
(632 days)
Product Code
Regulation Number
868.5630Type
TraditionalPanel
AnesthesiologyReference & Predicate Devices
N/A
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Device Name :
THE SWIRLER NEBULIZER
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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