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LENSSX LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K120732
510(k) Type
Traditional
Applicant
ALCON LENSX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2012
Days to Decision
181 days
Submission Type
Summary

LENSSX LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K120732
510(k) Type
Traditional
Applicant
ALCON LENSX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2012
Days to Decision
181 days
Submission Type
Summary