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WAVELIGHT FS200 PATIENT INTERFACE 1505

Page Type
Cleared 510(K)
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)
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