PMA P930014S165
- Device
- AcrySof® Posterior Chamber Intraocular Lens and Delivery Systems
- Applicant
- Alcon Laboratories, Inc.
- PMA number
- P930014
- Supplement
- S165
- Product code
- HQL
- Decision date
- 2026-07-02
- Classification
- Ophthalmic
- Generic name
- intraocular lens
- Approval order statement
- approval of ECH residual test method change at Alcon Research, LLC, WV USA
Current openFDA PMA Record#
- Device
- AcrySof® Posterior Chamber Intraocular Lens and Delivery Systems
- Applicant
- Alcon Laboratories, Inc.
- PMA number
- P930014
- Supplement
- S165
- Product code
- HQL
- Generic name
- intraocular lens
- Decision date
- 2026-07-02
- Decision code
- OK30
- Date received
- 2026-06-10
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- approval of ECH residual test method change at Alcon Research, LLC, WV USA