PMA P060022S025
- Device
- Akreos One-Piece Acrylic Intraocular Lens (IOL)
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P060022
- Supplement
- S025
- Product code
- HQL
- Decision date
- 2020-01-21
- Generic name
- intraocular lens
- Approval order statement
- Adding an alternative site for spectrometer testing of buttons.
Current openFDA PMA Record#
- Device
- Akreos One-Piece Acrylic Intraocular Lens (IOL)
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P060022
- Supplement
- S025
- Product code
- HQL
- Generic name
- intraocular lens
- Decision date
- 2020-01-21
- Decision code
- OK30
- Date received
- 2019-12-23
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- Adding an alternative site for spectrometer testing of buttons.