Last synced on 14 November 2025 at 11:06 pm

LenSx Laser System

Page Type
Cleared 510(K)
510(k) Number
K173660
510(k) Type
Traditional
Applicant
Alcon Laboratories, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/2018
Days to Decision
118 days
Submission Type
Summary

LenSx Laser System

Page Type
Cleared 510(K)
510(k) Number
K173660
510(k) Type
Traditional
Applicant
Alcon Laboratories, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/2018
Days to Decision
118 days
Submission Type
Summary