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LENSX LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K101626
510(k) Type
Traditional
Applicant
LENSX LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2010
Days to Decision
131 days
Submission Type
Summary

LENSX LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K101626
510(k) Type
Traditional
Applicant
LENSX LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2010
Days to Decision
131 days
Submission Type
Summary