FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Excimer Laser System
PMA: P020050
·
Supplement: S001
·
Decision Jun 4, 2004
Classifications
1
FEI Numbers
9
Registration Numbers
10
Basic Information
- Device Name
- Excimer Laser System
- Trade Name
- WAVELIGHT ALLEGRETTO WAVE EXCIMER LASER SYSTEM
- PMA Number
- P020050
- Supplement Number
- S001
- 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
- June 4, 2004
- Date Received
- May 21, 2004
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Express GMP Supplement
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR A MANUFACTURING SITE LOCATED AT WAVELIGHT LASER TECHNOLOGIE AG, PRESSATH, GERMANY.
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| LZS | Excimer Laser System | FDA class 3 | Unknown |