FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Intraocular Lens
PMA: P830033
·
Supplement: S027
·
Decision Jan 29, 1996
Classifications
1
FEI Numbers
59
Registration Numbers
59
Basic Information
- Device Name
- Intraocular Lens
- Trade Name
- SINGLE-PIECE AND THREE PIECE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER INTRAOCULAR LENSES (IOLS)
- PMA Number
- P830033
- Supplement Number
- S027
- 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
- January 29, 1996
- Date Received
- July 28, 1994
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
APPROVAL TO CHANGE VENDORS OF THE POLYMETHYLMETHACRYLATE (PMMA) MATERIAL USED TO MANUFACTURE IOLS APROVED UNDER THIS PMA AND ITS SUPPLEMENTS
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 |