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VISULUX

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161607
510(k) Type
Traditional
Applicant
Carl Zeiss Meditec, AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
2/23/2017
Days to Decision
258 days
Submission Type
Summary

VISULUX

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161607
510(k) Type
Traditional
Applicant
Carl Zeiss Meditec, AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
2/23/2017
Days to Decision
258 days
Submission Type
Summary