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LENSAR LASER SYSTEM - FS 3D FOR CORNEAL INCISIONS

Page Type
Cleared 510(K)
510(k) Number
K122829
510(k) Type
Traditional
Applicant
LENSAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/2012
Days to Decision
77 days
Submission Type
Summary

LENSAR LASER SYSTEM - FS 3D FOR CORNEAL INCISIONS

Page Type
Cleared 510(K)
510(k) Number
K122829
510(k) Type
Traditional
Applicant
LENSAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/2012
Days to Decision
77 days
Submission Type
Summary