PMA P040020S107
- Device
- AcrySof® IQ ReSTOR® Posterior Chamber Intraocular Lenses
- Applicant
- Alcon Research, Ltd.
- PMA number
- P040020
- Supplement
- S107
- Product code
- MFK
- Decision date
- 2024-05-29
- Classification
- Ophthalmic
- Generic name
- Lens, multifocal intraocular
- Approval order statement
- approval for a new Gas Chromatography (GC) ratio instrument method for AcrySof® & Clareon® Intraocular Lenses
Current openFDA PMA Record#
- Device
- AcrySof® IQ ReSTOR® Posterior Chamber Intraocular Lenses
- Applicant
- Alcon Research, Ltd.
- PMA number
- P040020
- Supplement
- S107
- Product code
- MFK
- Generic name
- Lens, multifocal intraocular
- Decision date
- 2024-05-29
- Decision code
- APPR
- Date received
- 2023-12-07
- Supplement type
- 135 Review Track For 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- approval for a new Gas Chromatography (GC) ratio instrument method for AcrySof® & Clareon® Intraocular Lenses