FDA PMA
FDA Class 2
Approved
🇺🇸 United States
Laser, Neodymium:Yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla
PMA: P830064
·
Supplement: S002
·
Decision Dec 13, 1984
Classifications
1
FEI Numbers
3
Registration Numbers
4
Basic Information
- Device Name
- Laser, Neodymium:Yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla
- Trade Name
- NEODYMIUM-YAG OP LASER OPL-3
- PMA Number
- P830064
- Supplement Number
- S002
- Device Class
- FDA Class 2
- Product Code
- LXS
- Generic Name
- Laser, neodymium:Yag, ophthalmic for posterior capsulotomy and cutting pupilla
- Regulation Number
- 886.4392
- Medical Specialty
- Ophthalmic
- Advisory Committee
- Ophthalmic
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- December 13, 1984
- Date Received
- November 7, 1984
- Expedited Review
- N
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 |
|---|---|---|---|
| LXS | Laser, Neodymium:Yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla | FDA class 2 | Ophthalmic |