PMA P060022S015
- Device
- AKREOS INTRAOCULAR LENS
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P060022
- Supplement
- S015
- Product code
- HQL
- Decision date
- 2013-03-26
- Generic name
- intraocular lens
- Approval order statement
- ADDITION OF AN ALTERNATE COMPONENT SUPPLIER.
Current openFDA PMA Record#
- Device
- AKREOS INTRAOCULAR LENS
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P060022
- Supplement
- S015
- Product code
- HQL
- Generic name
- intraocular lens
- Decision date
- 2013-03-26
- Decision code
- OK30
- Date received
- 2013-02-22
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- ADDITION OF AN ALTERNATE COMPONENT SUPPLIER.