PMA P930014S142
- Device
- AcrySof Posterior Chamber Intraocular Lens and Delivery Systems
- Applicant
- Alcon Laboratories, Inc.
- PMA number
- P930014
- Supplement
- S142
- Product code
- HQL
- Decision date
- 2022-03-25
- Generic name
- intraocular lens
- Approval order statement
- Modification to the testing frequency of the acrylate monomer inhibitor removal in-process test.
Current openFDA PMA Record#
- Device
- AcrySof Posterior Chamber Intraocular Lens and Delivery Systems
- Applicant
- Alcon Laboratories, Inc.
- PMA number
- P930014
- Supplement
- S142
- Product code
- HQL
- Generic name
- intraocular lens
- Decision date
- 2022-03-25
- Decision code
- OK30
- Date received
- 2022-03-01
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- Modification to the testing frequency of the acrylate monomer inhibitor removal in-process test.