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510(k) Data Aggregation
K Number
K960096Device Name
ULTRA IIIManufacturer
Date Cleared
1996-03-27
(76 days)
Regulation Number
890.5850Type
TraditionalPanel
Physical MedicineReference & Predicate Devices
N/A
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Device Name :
ULTRA III
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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