PMA P060022S008
- Device
- AKREOS POSTERIOR CHAMBER INTRACULAR LENS
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P060022
- Supplement
- S008
- Product code
- HQL
- Decision date
- 2011-04-29
- Generic name
- intraocular lens
- Approval order statement
- APPROVAL TO IMPLEMENT THE PROPOSED CHANGE TO THE BIOBURDEN TESTING FOR THE AKREOS POSTERIOR CHAMBER INTRAOCULAR LENS.
Current openFDA PMA Record#
- Device
- AKREOS POSTERIOR CHAMBER INTRACULAR LENS
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P060022
- Supplement
- S008
- Product code
- HQL
- Generic name
- intraocular lens
- Decision date
- 2011-04-29
- Decision code
- APPR
- Date received
- 2011-03-18
- Supplement type
- 135 Review Track For 30-Day Notice
- Approval order statement
- APPROVAL TO IMPLEMENT THE PROPOSED CHANGE TO THE BIOBURDEN TESTING FOR THE AKREOS POSTERIOR CHAMBER INTRAOCULAR LENS.