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510(k) Data Aggregation
K Number
K000861Device Name
CRANIOCAPManufacturer
Date Cleared
2000-10-30
(227 days)
Product Code
Regulation Number
882.5970Type
TraditionalPanel
NeurologyReference & Predicate Devices
N/A
Predicate For
N/A
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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