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 of procedures to add lens finishing laboratories as manufacturers and distributors of class iii rgp extended wear contact lenses.
| Device | MENICON SF-P (TM) |
| Classification Name | Lens, Contact (other Material) - Daily |
| Generic Name | Lens, Contact (other Material) - Daily |
| Applicant | MENICON CO. LTD. |
| Date Received | 2000-06-13 |
| Decision Date | 2000-09-06 |
| PMA | P880098 |
| Supplement | S011 |
| Product Code | HQD |
| Advisory Committee | Ophthalmic |
| Supplement Type | Normal 180 Day Track |
| Supplement Reason | Postapproval Study Protocol - Ode/oir |
| Expedited Review | No |
| Combination Product | No |
| Applicant Address | MENICON CO. LTD. 269a Ballardvale St. wilmington, MA 01887 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P880098 | Original Filing | |
| S012 | 2002-11-19 | Real-time Process |
| S011 | 2000-06-13 | Normal 180 Day Track |
| S010 | 1997-06-30 | Normal 180 Day Track |
| S009 | 1996-01-04 | Normal 180 Day Track |
| S008 | 1995-05-15 | Special (immediate Track) |
| S007 | ||
| S006 | 1993-03-01 | Normal 180 Day Track |
| S005 | 1991-08-08 | Normal 180 Day Track |
| S004 | 1990-02-13 | Normal 180 Day Track |
| S003 | 1989-12-01 | Normal 180 Day Track |
| S002 | 1989-10-06 | Normal 180 Day Track |
| S001 | 1989-07-24 | Normal 180 Day Track |