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510(k) Data Aggregation
K Number
K010897Device Name
MERIDIAN-PORTABLEManufacturer
Date Cleared
2001-06-19
(85 days)
Product Code
Regulation Number
882.1540Type
TraditionalPanel
NeurologyReference & Predicate Devices
N/A
Why did this record match?
Device Name :
MERIDIAN-PORTABLE
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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