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VICTUS FEMTOSECOND LASER PLATFORM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132534
510(k) Type
Traditional
Applicant
Technolas Perfect Vision GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2014
Days to Decision
185 days
Submission Type
Summary

VICTUS FEMTOSECOND LASER PLATFORM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132534
510(k) Type
Traditional
Applicant
Technolas Perfect Vision GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2014
Days to Decision
185 days
Submission Type
Summary