Last synced on 14 November 2025 at 11:06 pm

RxSight Insertion Device

Page Type
Cleared 510(K)
510(k) Number
K192926
510(k) Type
Traditional
Applicant
RxSight, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2020
Days to Decision
93 days
Submission Type
Summary

RxSight Insertion Device

Page Type
Cleared 510(K)
510(k) Number
K192926
510(k) Type
Traditional
Applicant
RxSight, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2020
Days to Decision
93 days
Submission Type
Summary