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510(k) Data Aggregation
K Number
K011229Device Name
DEVILBISS 9000 SERIES CPAP, MODEL 9001Manufacturer
Date Cleared
2001-07-11
(79 days)
Product Code
Regulation Number
868.5905Type
SpecialPanel
AnesthesiologyReference & Predicate Devices
N/A
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Device Name :
DEVILBISS 9000 SERIES CPAP, MODEL 9001
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
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