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.
New sterilizer for production use.
Device | PMMA ANTERIOR CHAMBER IOLS |
Generic Name | Intraocular Lens |
Applicant | ALCON LABORATORIES |
Date Received | 2006-07-24 |
Decision Date | 2006-08-24 |
PMA | P880087 |
Supplement | S012 |
Product Code | HQL |
Advisory Committee | Ophthalmic |
Supplement Type | 30-day Notice |
Supplement Reason | Process Change - Manufacturer/sterilizer/packager/supplier |
Expedited Review | No |
Combination Product | No |
Applicant Address | ALCON LABORATORIES 6201 S Freeway ft Worth, TX 76134 |
Supplement Number | Date | Supplement Type |
---|---|---|
P880087 | Original Filing | |
S031 | 2021-06-21 | Normal 180 Day Track No User Fee |
S030 | 2020-11-25 | 30-day Notice |
S029 | 2019-07-05 | 30-day Notice |
S028 | 2019-03-25 | 30-day Notice |
S027 | 2019-03-25 | 30-day Notice |
S026 | 2016-11-30 | 30-day Notice |
S025 | 2016-08-03 | 30-day Notice |
S024 | ||
S023 | 2015-12-09 | 30-day Notice |
S022 | 2013-04-22 | 30-day Notice |
S021 | 2012-12-26 | Normal 180 Day Track No User Fee |
S020 | 2012-10-01 | 30-day Notice |
S019 | 2011-06-24 | 30-day Notice |
S018 | 2010-08-25 | 30-day Notice |
S017 | 2010-08-10 | 30-day Notice |
S016 | 2010-05-03 | 30-day Notice |
S015 | 2010-05-03 | 30-day Notice |
S014 | 2009-12-24 | 30-day Notice |
S013 | 2009-06-30 | 30-day Notice |
S012 | 2006-07-24 | 30-day Notice |
S011 | 2004-10-18 | 135 Review Track For 30-day Notice |
S010 | 2004-04-16 | Real-time Process |
S009 | 1996-10-24 | Normal 180 Day Track |
S008 | ||
S007 | 1996-08-08 | Normal 180 Day Track |
S006 | 1995-08-09 | Normal 180 Day Track |
S005 | 1995-01-31 | Normal 180 Day Track |
S004 | 1991-08-21 | Normal 180 Day Track |
S003 | ||
S002 | 1990-03-26 | Normal 180 Day Track |
S001 |