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MODEL VISULAS 532S LASER WITH THE VITE OPTION

Page Type
Cleared 510(K)
510(k) Number
K100035
510(k) Type
Special
Applicant
CARL ZEISS MEDITEC AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/17/2010
Days to Decision
70 days
Submission Type
Summary

MODEL VISULAS 532S LASER WITH THE VITE OPTION

Page Type
Cleared 510(K)
510(k) Number
K100035
510(k) Type
Special
Applicant
CARL ZEISS MEDITEC AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/17/2010
Days to Decision
70 days
Submission Type
Summary