Atlas FDA

WaveLlght EX500 Laser System

FDA premarket approval P020050/S037 · decided 2021-02-18

Approval details

PMA number
P020050
Supplement
S037
Supplement type
Special (Immediate Track)
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
WaveLlght EX500 Laser System
Generic name
Excimer laser system
Applicant
Alcon Laboratories, Inc.
Date received
2021-01-19
Decision date
2021-02-18
Days to decision
30 days
Decision code
APPR
Product code
LZS
Advisory committee
Ophthalmic
Expedited review
No
Location
Fort Worth, TX
Statement
Approval for labeling changes to add and strengthen contraindications.

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510(k) clearances by this applicant

RecordFirmDate
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UNITY VCS (8065000296); UNITY CS (8065000297) (K233876)Alcon Laboratories, Inc.2024-06-21
Centurion™ Vision System (Active Sentry™) (8065753057) (K233902)Alcon Laboratories, Inc.2024-01-10
Precision1; Precision1 for Astigmatism; TOTAL30; TOTAL30 for Astigmatism; TOTAL30 Multifocal (K233856)Alcon Laboratories, Inc.2023-12-29