Last synced on 9 May 2025 at 11:05 pm

VISULAS combi

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233911
510(k) Type
Traditional
Applicant
Carl Zeiss Meditec AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
9/6/2024
Days to Decision
269 days
Submission Type
Summary

VISULAS combi

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233911
510(k) Type
Traditional
Applicant
Carl Zeiss Meditec AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
9/6/2024
Days to Decision
269 days
Submission Type
Summary