FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Intraocular Lens
PMA: P860059
·
Supplement: S076
·
Decision Sep 17, 1996
Classifications
1
FEI Numbers
59
Registration Numbers
59
Basic Information
- Device Name
- Intraocular Lens
- Trade Name
- TIER A LENS MODELS UPB360GN AND UP320F
- PMA Number
- P860059
- Supplement Number
- S076
- Device Class
- FDA Class 3
- Product Code
- HQL
- Generic Name
- intraocular lens
- Regulation Number
- 886.3600
- Medical Specialty
- Ophthalmic
- Advisory Committee
- Ophthalmic
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- September 17, 1996
- Date Received
- April 5, 1996
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
APPROVAL OF MODELS UPB360GN AND UP320F AS TIER A MODIFICATIONS OF PREVIOUSLY APPROVED PARENT IOLS. MODEL UPB360GN WILL BE MARKETED UNDER THE TRADE NAME TOP NOTCH
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 |
|---|---|---|---|
| HQL | Intraocular Lens | FDA class 3 | Ophthalmic |