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WAVELIGHT FS200 PATIENT INTERFACE 1505

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121031
510(k) Type
Abbreviated
Applicant
ALCON RESEARCH, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/21/2012
Days to Decision
77 days
Submission Type
Summary

WAVELIGHT FS200 PATIENT INTERFACE 1505

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121031
510(k) Type
Abbreviated
Applicant
ALCON RESEARCH, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/21/2012
Days to Decision
77 days
Submission Type
Summary