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WaveLight FS200 Patient Interface

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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