PMA P880087S016
- Device
- ACRYSOF INTRAOCULAR LENSES
- Applicant
- Alcon Laboratories
- PMA number
- P880087
- Supplement
- S016
- Product code
- HQL
- Decision date
- 2010-06-02
- Generic name
- intraocular lens
- Approval order statement
- ELIMINATION OF A QUALITY CONTROL TEST DURING MANUFACTURING OF THE DEVICE.
Current openFDA PMA Record#
- Device
- ACRYSOF INTRAOCULAR LENSES
- Applicant
- Alcon Laboratories
- PMA number
- P880087
- Supplement
- S016
- Product code
- HQL
- Generic name
- intraocular lens
- Decision date
- 2010-06-02
- Decision code
- OK30
- Date received
- 2010-05-03
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- ELIMINATION OF A QUALITY CONTROL TEST DURING MANUFACTURING OF THE DEVICE.