PMA P060022S022
- Device
- AKREOS INTRAOCULAR LENS
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P060022
- Supplement
- S022
- Product code
- HQL
- Decision date
- 2016-03-11
- Generic name
- intraocular lens
- Approval order statement
- Approval for the addition of an alternate packaging component supplier for the Akreos Plastic Vial Components.
Current openFDA PMA Record#
- Device
- AKREOS INTRAOCULAR LENS
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P060022
- Supplement
- S022
- Product code
- HQL
- Generic name
- intraocular lens
- Decision date
- 2016-03-11
- Decision code
- APPR
- Date received
- 2015-09-11
- Supplement type
- 135 Review Track For 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- Approval for the addition of an alternate packaging component supplier for the Akreos Plastic Vial Components.