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 | MODELS 1S & 1P |
Generic Name | intraocular lens |
Regulation Number | 886.3600 |
Applicant | ALCON 6201 South Freeway Fort Worth, TX 76134-2099 |
PMA Number | P800049 |
Supplement Number | S004 |
Date Received | 07/10/1991 |
Decision Date | 05/29/1992 |
Withdrawal Date
|
12/23/2004 |
Product Code |
HQL |
Advisory Committee |
Ophthalmic |
Supplement Type | Normal 180 Day Track |
Supplement Reason | Location Change - Manufacturer/Sterilizer/Packager/Supplier |
Expedited Review Granted? | No |
Combination Product | No |
|
|