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510(k) Data Aggregation
K Number
K010057Device Name
MODIFICATION TO ARTOSCAN MManufacturer
Date Cleared
2001-02-02
(25 days)
Product Code
Regulation Number
892.1000Type
SpecialPanel
Radiology (RA)Reference & Predicate Devices
N/A
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Device Name :
MODIFICATION TO ARTOSCAN M
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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