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510(k) Data Aggregation
K Number
K001980Manufacturer
Date Cleared
2000-09-27
(90 days)
Product Code
Regulation Number
882.1320Type
TraditionalPanel
NeurologyReference & Predicate Devices
N/A
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Device Name :
ASPECT MEDICAL SYSTEMS PEDIATRIC BIS EEG SENSOR, MODEL 186-0110
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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