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 | RIGID GAS PERMEABLE CONTACT LENSES |
Generic Name | Lens, Contact (other Material) - Daily |
Applicant | THE LIFESTYLE CO., INC. |
Date Received | 1992-03-04 |
Decision Date | 1992-04-14 |
PMA | P900001 |
Supplement | S005 |
Product Code | HQD |
Advisory Committee | Ophthalmic |
Supplement Type | Normal 180 Day Track |
Supplement Reason | Location Change - Manufacturer/sterilizer/packager/supplier |
Expedited Review | No |
Combination Product | No |
Applicant Address | THE LIFESTYLE CO., INC. 712 Ginesi Dr. morganville, NJ 07751 |
Supplement Number | Date | Supplement Type |
---|---|---|
P900001 | Original Filing | |
S009 | 1993-05-11 | Normal 180 Day Track |
S008 | 1992-11-06 | Normal 180 Day Track |
S007 | 1992-09-23 | Normal 180 Day Track |
S006 | 1992-08-19 | Normal 180 Day Track |
S005 | 1992-03-04 | Normal 180 Day Track |
S004 | 1991-12-23 | Normal 180 Day Track |
S003 | 1991-07-16 | Normal 180 Day Track |
S002 | 1991-04-11 | Normal 180 Day Track |
S001 | 1991-02-08 | 30-Day Supplement |
Device ID | PMA | Supp |
---|---|---|
00830002003019 | P900001 | 001 |