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510(k) Data Aggregation

K Number

Device Name

RETeval Visual Electrodiagnostic Device

Manufacturer

LKC Technologies, Inc

Date Cleared

2015-05-19

(249 days)

Product Code

GWE

Regulation Number

882.1890

Why did this record match?

Applicant Name (Manufacturer) :

LKC Technologies, Inc

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized

Intended Use

Device Description

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