FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Intraocular Lens
PMA: P930014
·
Supplement: S024
·
Decision Feb 5, 2009
Classifications
1
FEI Numbers
59
Registration Numbers
59
Basic Information
- Device Name
- Intraocular Lens
- Trade Name
- ACRYSERT DELIVERY SYSTEM
- PMA Number
- P930014
- Supplement Number
- S024
- 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
- February 5, 2009
- Date Received
- April 21, 2008
- Supplement Type
- Real-Time Process
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
APPROVAL OF THE ACRYSERT DELIVERY SYSTEM WITH THE ACRYSOF IQ IOL MODEL SN60WS.
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 |