PMA P060022S004
- Device
- AKREOS POSTERIOR CHAMBER INTRAOCULAR LENS
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P060022
- Supplement
- S004
- Product code
- HQL
- Decision date
- 2009-04-03
- Generic name
- intraocular lens
- Approval order statement
- ALTERNATE MEASUREMENT SYSTEM FOR MEASURING THE AKREOS LENS HAPTICS.
Current openFDA PMA Record#
- Device
- AKREOS POSTERIOR CHAMBER INTRAOCULAR LENS
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P060022
- Supplement
- S004
- Product code
- HQL
- Generic name
- intraocular lens
- Decision date
- 2009-04-03
- Decision code
- OK30
- Date received
- 2009-03-06
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- ALTERNATE MEASUREMENT SYSTEM FOR MEASURING THE AKREOS LENS HAPTICS.