FDA PMA FDA Class 3 Approved 🇺🇸 United States

Excimer Laser System

PMA: P020050 · Supplement: S044 · Decision Jan 16, 2025
Classifications
1
FEI Numbers
9
Registration Numbers
10

Basic Information

Device Name
Excimer Laser System
Trade Name
WaveLight EX500 Laser System
PMA Number
P020050
Supplement Number
S044
Device Class
FDA Class 3
Product Code
LZS
Generic Name
Excimer laser system
Medical Specialty
Unknown
Advisory Committee
Ophthalmic
Decision
Approved
Decision Code
APPR
Decision Date
January 16, 2025
Date Received
October 22, 2024
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for an alternate joystick in the Patient Bed Swivel 1125 of the WaveLight EX500 Laser System

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LZS Excimer Laser System