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VX130 Ophthalmic Diagnostic Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162067
510(k) Type
Traditional
Applicant
LUNEAU SAS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
4/24/2017
Days to Decision
272 days
Submission Type
Summary

VX130 Ophthalmic Diagnostic Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162067
510(k) Type
Traditional
Applicant
LUNEAU SAS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
4/24/2017
Days to Decision
272 days
Submission Type
Summary