Last synced on 20 December 2024 at 11:05 pm

VX120 Ophthalmic Diagnostic Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143086
510(k) Type
Traditional
Applicant
LUNEAU SAS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
6/1/2015
Days to Decision
217 days
Submission Type
Summary

VX120 Ophthalmic Diagnostic Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143086
510(k) Type
Traditional
Applicant
LUNEAU SAS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
6/1/2015
Days to Decision
217 days
Submission Type
Summary