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RxSight Insertion Device

Page Type
Cleared 510(K)
510(k) Number
K181401
510(k) Type
Traditional
Applicant
RxSight, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2018
Days to Decision
58 days
Submission Type
Summary

RxSight Insertion Device

Page Type
Cleared 510(K)
510(k) Number
K181401
510(k) Type
Traditional
Applicant
RxSight, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2018
Days to Decision
58 days
Submission Type
Summary