PMA P060022S038
- Device
- Akreos posterior chamber intraocular lens
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P060022
- Supplement
- S038
- Product code
- HQL
- Decision date
- 2026-09-03
- Classification
- Ophthalmic
- Generic name
- intraocular lens
- Approval order statement
- the elimination of certain redundant post-coating incoming inspections for coated lens shuttles
Current openFDA PMA Record#
- Device
- Akreos posterior chamber intraocular lens
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P060022
- Supplement
- S038
- Product code
- HQL
- Generic name
- intraocular lens
- Decision date
- 2026-09-03
- Decision code
- OK30
- Date received
- 2026-08-10
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- the elimination of certain redundant post-coating incoming inspections for coated lens shuttles