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FDA 510(k) Applications Submitted by RxSight, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K231466
05/19/2023
RxSight Insertion Device
RxSight, Inc.
K181401
05/29/2018
RxSight Insertion Device
RxSight, Inc.
K201909
07/09/2020
RxSight Contact Lens
RxSight, Inc.
K192926
10/16/2019
RxSight Insertion Device
RxSight, Inc.
K231838
06/22/2023
RxSight« Insertion Device (63002)
RxSight, Inc.
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