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510(k) Data Aggregation
K Number
K010156Device Name
SLEEP PAT 200 DEVICEManufacturer
Date Cleared
2002-06-19
(519 days)
Product Code
Regulation Number
868.2375Type
TraditionalPanel
AnesthesiologyReference & Predicate Devices
N/A
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Device Name :
SLEEP PAT 200 DEVICE
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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