PMA P930014S119
- Device
- AcrySof Intraocular Lenses
- Applicant
- Alcon Laboratories, Inc.
- PMA number
- P930014
- Supplement
- S119
- Product code
- HQL
- Decision date
- 2019-03-14
- Classification
- Intraocular Lens
- Generic name
- intraocular lens
- Approval order statement
- Change an in-process quality control procedure associated with plasma treatments of the AcrySert and UltraSert Pre-loaded IOL Delivery Systems.
Current openFDA PMA Record#
- Device
- AcrySof Intraocular Lenses
- Applicant
- Alcon Laboratories, Inc.
- PMA number
- P930014
- Supplement
- S119
- Product code
- HQL
- Generic name
- intraocular lens
- Decision date
- 2019-03-14
- Decision code
- OK30
- Date received
- 2019-03-01
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- Change an in-process quality control procedure associated with plasma treatments of the AcrySert and UltraSert Pre-loaded IOL Delivery Systems.