FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Intraocular Lens
PMA: P930014
·
Supplement: S162
·
Decision Mar 2, 2026
Classifications
1
FEI Numbers
0
Registration Numbers
0
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Basic Information
- Device Name
- Intraocular Lens
- Trade Name
- AcrySof® Posterior Chamber Intraocular Lens and Delivery Systems
- PMA Number
- P930014
- Supplement Number
- S162
- Device Class
- FDA Class 3
- Product Code
- HQL
- Generic Name
- intraocular lens
- Regulation Number
- 886.3600
- Medical Specialty
- Ophthalmic
- Advisory Committee
- Ophthalmic
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- March 2, 2026
- Date Received
- February 3, 2026
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
addition of a new purified water system at the Alcon Huntington North Manufacturing Site
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 |