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510(k) Data Aggregation
K Number
K002040Device Name
FMS SOLOManufacturer
Date Cleared
2000-09-11
(68 days)
Product Code
Regulation Number
888.1100Type
TraditionalPanel
OrthopedicReference & Predicate Devices
N/A
Why did this record match?
Device Name :
FMS SOLO
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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