FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Femtosecond Laser System For Refractive Correction
PMA: P150040
·
Supplement: S001
·
Decision Feb 28, 2017
Classifications
1
FEI Numbers
2
Registration Numbers
2
Basic Information
- Device Name
- Femtosecond Laser System For Refractive Correction
- Trade Name
- VISUMAX FEMTOSECOND LASER SYSTEM
- PMA Number
- P150040
- Supplement Number
- S001
- Device Class
- FDA Class 3
- Product Code
- OTL
- Generic Name
- Femtosecond laser system for refractive correction
- Medical Specialty
- Unknown
- Advisory Committee
- Ophthalmic
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- February 28, 2017
- Date Received
- January 6, 2017
- Supplement Type
- Real-Time Process
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
Approval for software changes.
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 |
|---|---|---|---|
| OTL | Femtosecond Laser System For Refractive Correction | FDA class 3 | Unknown |