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510(k) Data Aggregation
K Number
K000122Manufacturer
Date Cleared
2001-09-20
(611 days)
Product Code
Regulation Number
888.3045Type
TraditionalPanel
OrthopedicReference & Predicate Devices
N/A
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Applicant Name (Manufacturer) :
NEUCOLL, INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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