Atlas FDA

WaveLight EX500 Laser

FDA premarket approval P020050/S042 · decided 2024-02-15

Approval details

PMA number
P020050
Supplement
S042
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
WaveLight EX500 Laser
Generic name
Excimer laser system
Applicant
Alcon Laboratories, Inc.
Date received
2023-09-05
Decision date
2024-02-15
Days to decision
163 days
Decision code
APPR
Product code
LZS
Advisory committee
Ophthalmic
Expedited review
No
Location
Fort Worth, TX
Statement
hardware design changes for the WaveLight Ex500 Laser

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510(k) clearances by this applicant

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