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510(k) Data Aggregation
K Number
K964360Manufacturer
Date Cleared
1997-04-04
(154 days)
Product Code
Regulation Number
868.1880Type
TraditionalPanel
AnesthesiologyReference & Predicate Devices
N/A
Why did this record match?
Device Name :
VENT(VENTCHECK) HANDHELD RESPIRATORY/MECHANICS MONITOR MODEL 101
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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