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510(k) Data Aggregation
K Number
K964806Device Name
MD-1835Manufacturer
Date Cleared
1997-03-04
(95 days)
Product Code
Regulation Number
892.1670Type
TraditionalPanel
RadiologyReference & Predicate Devices
N/A
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Device Name :
MD-1835
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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