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VX120 Ophthalmic Diagnostic Device

Page Type
Cleared 510(K)
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)
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