PMA P060022S026
- Device
- Akreos Posterior Chamber Intraocular Lens
- Applicant
- Bausch & Lomb, Inc.
- Product code
- HQL
- Decision date
- 2021-05-04
- Generic name
- intraocular lens
- Approval order statement
- Approval for changes to the packaging of preloaded Akreos intraocular lens models AO60 and MI60.
Current openFDA PMA Record#
- Device
- Akreos Posterior Chamber Intraocular Lens
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P060022
- Supplement
- S026
- Product code
- HQL
- Generic name
- intraocular lens
- Decision date
- 2021-05-04
- Decision code
- APPR
- Date received
- 2020-08-28
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- Approval for changes to the packaging of preloaded Akreos intraocular lens models AO60 and MI60.