PMA P060022S024
- Device
- Akreos Intraocular Lens
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P060022
- Supplement
- S024
- Product code
- HQL
- Decision date
- 2018-08-07
- Classification
- Intraocular Lens
- Generic name
- intraocular lens
- Approval order statement
- Adding a mask to the polishing procedure for manufacturing the Akreos Intraocular Lens, Models AO60 and MI60L.
Current openFDA PMA Record#
- Device
- Akreos Intraocular Lens
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P060022
- Supplement
- S024
- Product code
- HQL
- Generic name
- intraocular lens
- Decision date
- 2018-08-07
- Decision code
- OK30
- Date received
- 2018-07-10
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- Adding a mask to the polishing procedure for manufacturing the Akreos Intraocular Lens, Models AO60 and MI60L.