PMA P060022S012
- Device
- AKREOS POSTERIOR CHAMBER INTRAOCULAR LENS
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P060022
- Supplement
- S012
- Product code
- HQL
- Decision date
- 2012-06-18
- Generic name
- intraocular lens
- Approval order statement
- APPROVAL FOR MODIFICATIONS TO THE PRIMARY PACKAGING WHICH INCLUDES AN ALTERNATE PLASTIC VIAL AND INTRAOCULAR LENS (IOL) HOLDER.
Current openFDA PMA Record#
- Device
- AKREOS POSTERIOR CHAMBER INTRAOCULAR LENS
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P060022
- Supplement
- S012
- Product code
- HQL
- Generic name
- intraocular lens
- Decision date
- 2012-06-18
- Decision code
- APPR
- Date received
- 2011-06-21
- Supplement type
- Normal 180 Day Track
- Approval order statement
- APPROVAL FOR MODIFICATIONS TO THE PRIMARY PACKAGING WHICH INCLUDES AN ALTERNATE PLASTIC VIAL AND INTRAOCULAR LENS (IOL) HOLDER.