Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information. |
|
Device | AcrySof Posterior Chamber Intraocular Lens and Delivery Systems |
Generic Name | intraocular lens |
Regulation Number | 886.3600 |
Applicant | ALCON LABORATORIES, INC. 6201 SOUTH FREEWAY DR. FORT WORTH, TX 76134 |
PMA Number | P930014 |
Supplement Number | S123 |
Date Received | 07/05/2019 |
Decision Date | 08/01/2019 |
Product Code |
HQL |
Advisory Committee |
Ophthalmic |
Supplement Type | 30-Day Notice |
Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement Addition of a 100% Ethylene Oxide (EO) sterilization chamber, integrated aeration cell, and supporting equipment at the Alcon Huntington manufacturing facility. |
|
|