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VISUMAX LASER KERATOME

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100253
510(k) Type
Traditional
Applicant
CARL ZEISS MEDITEC AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/2010
Days to Decision
161 days
Submission Type
Summary

VISUMAX LASER KERATOME

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100253
510(k) Type
Traditional
Applicant
CARL ZEISS MEDITEC AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/2010
Days to Decision
161 days
Submission Type
Summary