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ALCON LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023249
510(k) Type
Abbreviated
Applicant
ALCON LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2002
Days to Decision
18 days
Submission Type
Summary

ALCON LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023249
510(k) Type
Abbreviated
Applicant
ALCON LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2002
Days to Decision
18 days
Submission Type
Summary