K Number
K953117

Validate with FDA (Live)

Device Name
SCANMASTER DX
Manufacturer
Date Cleared
1996-01-18

(199 days)

Product Code
Regulation Number
892.2030
Age Range
N/A
Reference & Predicate Devices
N/A
Predicate For
N/A
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview

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N/A