FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Intraocular Lens
PMA: P840039
·
Supplement: S049
·
Decision Jun 5, 1996
Classifications
1
FEI Numbers
59
Registration Numbers
59
Basic Information
- Device Name
- Intraocular Lens
- Trade Name
- ONE PIECE POSTERIOR CHAMBER IOL
- PMA Number
- P840039
- Supplement Number
- S049
- 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
- June 5, 1996
- Date Received
- December 19, 1995
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
APPROVAL TO EXTEND THE POWER RANGE FOR YOUR ONE-PIECE POSTERIOR CHAMBER IOLS FORM (+4.0 D) - (+34 D) TO (-18.0 D) - (+45 D).
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 |