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.
Approval for an alternate biological indicator, the 3m attest rapid readout biological indicator, to monitor the sterilization processes and to use only the fluorescent enzyme 3 hour readout system for routine disposition of the product. The fluorescent readout system by itself will not be used to validate the sterilization processes.
| Device | BAUSCH AND LOMB ALPHAFILCON A HYDROPHILIC CONTACT LENSES |
| Generic Name | Lenses, Soft Contact, Extended Wear |
| Applicant | Bausch & Lomb, Inc. |
| Date Received | 2001-01-09 |
| Decision Date | 2002-06-28 |
| PMA | P960022 |
| Supplement | S002 |
| Advisory Committee | Ophthalmic |
| Supplement Type | Normal 180 Day Track |
| Supplement Reason | Change Design/components/specifications/material |
| Expedited Review | No |
| Combination Product | No |
| Applicant Address | Bausch & Lomb, Inc. 1400 North Goodman St. rochester, NY 14609-3547 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P960022 | Original Filing | |
| S012 | 2020-03-20 | 30-day Notice |
| S011 | 2015-09-29 | 30-day Notice |
| S010 | 2013-10-17 | 30-day Notice |
| S009 | 2011-10-19 | 135 Review Track For 30-day Notice |
| S008 | 2011-03-03 | 30-day Notice |
| S007 | 2010-11-15 | Normal 180 Day Track No User Fee |
| S006 | 2010-05-17 | 30-day Notice |
| S005 | 2008-09-24 | Real-time Process |
| S004 | 2004-02-06 | 30-day Notice |
| S003 | 2003-03-03 | Real-time Process |
| S002 | 2001-01-09 | Normal 180 Day Track |
| S001 | 1997-08-07 | Normal 180 Day Track |