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510(k) Data Aggregation
K Number
K955084Device Name
ASPACH 65,000 (MODIFICATION)Manufacturer
Date Cleared
1996-01-17
(90 days)
Product Code
Regulation Number
878.4820Type
TraditionalPanel
OrthopedicReference & Predicate Devices
N/A
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Device Name :
ASPACH 65,000 (MODIFICATION)
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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