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WAVELIGHT FS200 LASER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141476
510(k) Type
Traditional
Applicant
ALCON RESEARCH, LTD. DBA ALCON LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/2014
Days to Decision
118 days
Submission Type
Summary

WAVELIGHT FS200 LASER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141476
510(k) Type
Traditional
Applicant
ALCON RESEARCH, LTD. DBA ALCON LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/2014
Days to Decision
118 days
Submission Type
Summary