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510(k) Data Aggregation
K Number
K003525Device Name
VOLUSON 730 DIAGNOSTIC ULTRASOUND SYSTEMManufacturer
Date Cleared
2000-11-22
(7 days)
Regulation Number
892.1550Type
TraditionalPanel
Radiology (RA)Reference & Predicate Devices
N/A
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Device Name :
VOLUSON 730 DIAGNOSTIC ULTRASOUND SYSTEM
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
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