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WAVELIGHT EX500 EXCIMER LASER SYSTEM

FDA premarket approval P020050/S015 · decided 2014-04-10

Approval details

PMA number
P020050
Supplement
S015
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
WAVELIGHT EX500 EXCIMER LASER SYSTEM
Generic name
Excimer laser system
Applicant
Alcon Laboratories, Inc.
Date received
2014-01-22
Decision date
2014-04-10
Days to decision
78 days
Decision code
APPR
Product code
LZS
Advisory committee
Ophthalmic
Expedited review
No
Location
Fort Worth, TX
Statement
APPROVAL FOR AN ALTERNATE MODIFIED PATIENT SWIVEL BED FOR USE WITH THE WAVELIGHT® EX500 EXCIMER LASER SYSTEM. THE MODIFICATIONS ALLOW THE PATIENT BED TO BE USED WITH FEMTOSECOND LASERS OTHER THAN THE WAVELIGHT FS200 LASER TO CREATE THE FLAP FOR LASER-ASSISTED IN SITU KERATOMILEUSIS (LASIK).

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