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LENSX 550 LASER SYSTEM. MODEL 550

Page Type
Cleared 510(K)
510(k) Number
K094052
510(k) Type
Traditional
Applicant
LENSX LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/2010
Days to Decision
113 days
Submission Type
Summary

LENSX 550 LASER SYSTEM. MODEL 550

Page Type
Cleared 510(K)
510(k) Number
K094052
510(k) Type
Traditional
Applicant
LENSX LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/2010
Days to Decision
113 days
Submission Type
Summary