PMA P060022S007
- Device
- AKREOS POSTERIOR CHAMBER INTRAOCULAR LENS
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P060022
- Supplement
- S007
- Product code
- HQL
- Decision date
- 2010-05-19
- Generic name
- intraocular lens
- Approval order statement
- ELIMINATION OF THE OPHTHALMIC IRRIGATION SOLUTION SPECIFICATION OF THE LENS STORAGE SOLUTION.
Current openFDA PMA Record#
- Device
- AKREOS POSTERIOR CHAMBER INTRAOCULAR LENS
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P060022
- Supplement
- S007
- Product code
- HQL
- Generic name
- intraocular lens
- Decision date
- 2010-05-19
- Decision code
- OK30
- Date received
- 2010-04-30
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- ELIMINATION OF THE OPHTHALMIC IRRIGATION SOLUTION SPECIFICATION OF THE LENS STORAGE SOLUTION.