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WaveLight FS200 Patient Interface

Page Type
Cleared 510(K)
510(k) Number
K190392
510(k) Type
Special
Applicant
Alcon Laboratories, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/2019
Days to Decision
35 days
Submission Type
Summary

WaveLight FS200 Patient Interface

Page Type
Cleared 510(K)
510(k) Number
K190392
510(k) Type
Special
Applicant
Alcon Laboratories, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/2019
Days to Decision
35 days
Submission Type
Summary