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510(k) Data Aggregation
K Number
K970439Device Name
PROXIDERM (D-460,D 90 460,D 180,460, PS 460)Manufacturer
Date Cleared
1997-04-16
(70 days)
Product Code
Regulation Number
878.4320Type
TraditionalReference & Predicate Devices
N/A
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Device Name :
PROXIDERM (D-460,D 90 460,D 180,460, PS 460)
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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