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RETeval Visual Electrodiagnostic Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142567
510(k) Type
Traditional
Applicant
LKC Technologies, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/2015
Days to Decision
249 days
Submission Type
Summary

RETeval Visual Electrodiagnostic Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142567
510(k) Type
Traditional
Applicant
LKC Technologies, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/2015
Days to Decision
249 days
Submission Type
Summary