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510(k) Data Aggregation

K Number

Device Name

ViMove

Manufacturer

dorsaVi Ltd.

Date Cleared

2015-05-28

(265 days)

Product Code

IKN, HCC, KQX

Regulation Number

890.1375

Why did this record match?

Applicant Name (Manufacturer) :

dorsaVi Ltd.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized

Intended Use

Device Description

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