PMA P060022S013
- Device
- AKREOS POSTERIOR CHAMBER INTRAOCULAR LENS (IOL)
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P060022
- Supplement
- S013
- Product code
- HQL
- Decision date
- 2012-05-16
- Generic name
- intraocular lens
- Approval order statement
- APPROVAL TO ADD TWO TABS TO THE HAPTICS OF THE MODEL M160 IOL.
Current openFDA PMA Record#
- Device
- AKREOS POSTERIOR CHAMBER INTRAOCULAR LENS (IOL)
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P060022
- Supplement
- S013
- Product code
- HQL
- Generic name
- intraocular lens
- Decision date
- 2012-05-16
- Decision code
- APPR
- Date received
- 2012-03-20
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Approval order statement
- APPROVAL TO ADD TWO TABS TO THE HAPTICS OF THE MODEL M160 IOL.