|Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.|
|Trade Name||AKREOS POSTERIOR CHAMBER INTRACULAR LENS|
|Classification Name||intraocular lens|
|Applicant||BAUSCH & LOMB, INC.|
|Supplement Type||135 review track for 30-day notice|
|Expedited Review Granted?|| No|
|Approval Order Statement |
Approval to implement the proposed change to the bioburden testing for the akreos posterior chamber intraocular lens.