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510(k) Data Aggregation

K Number

Device Name

R4 ACERT ULTRASOUND REPORTING SYSTEM

Manufacturer

Date Cleared

2011-09-15

(435 days)

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Applicant Name (Manufacturer) :

R4 LLC

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

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