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K Number
K001712

Validate with FDA (Live)

Device Name
3D ACTIVETRAC
Manufacturer
THE SAUNDERS GROUP
Date Cleared
2000-08-31

(87 days)

Product Code
ITH
Regulation Number
890.5900
Type
Traditional
Panel
Physical Medicine
Age Range
N/A
Reference & Predicate Devices
N/A
Predicate For
K023160,K031862,K031996,K040167,K042482,K051013,K071347,K073542,K083732,K101889,K965055,K970823,K981533,K992309,K992409
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview

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N/A