PMA P060022S001
- Device
- AKREOS POSTERIOR CHAMBER INTRAOCULAR LENS
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P060022
- Supplement
- S001
- Product code
- HQL
- Decision date
- 2008-11-19
- Generic name
- intraocular lens
- Approval order statement
- CHANGE IN SITE FOR THE BIOBURDEN AND ENDOTOXIN TESTING.
Current openFDA PMA Record#
- Device
- AKREOS POSTERIOR CHAMBER INTRAOCULAR LENS
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P060022
- Supplement
- S001
- Product code
- HQL
- Generic name
- intraocular lens
- Decision date
- 2008-11-19
- Decision code
- OK30
- Date received
- 2008-10-20
- Supplement type
- 30-Day Notice
- Approval order statement
- CHANGE IN SITE FOR THE BIOBURDEN AND ENDOTOXIN TESTING.