PMA supplement
P880098 S001: MENICON SF-P RGP (MELAFOCON A) CONTACT LENS
FDA PMA supplement · Normal 180 Day Track · Menicon Co, Ltd.
Key facts
| Original PMA | P880098 |
|---|---|
| Supplement number | S001 |
| Supplement type | Normal 180 Day Track |
| Reason for the supplement | Labeling Change - Indications/instructions/shelf life/tradename |
| Trade name | MENICON SF-P RGP (MELAFOCON A) CONTACT LENS |
| Generic name | Lenses, soft contact, daily wear |
| Applicant | Menicon Co, Ltd. |
| Product code | LPL |
| Received date | Jul 24, 1989 |
| Decision date | Feb 8, 1990 |
| Docket number | 90M-0068 |
| Notice date | Mar 8, 1990 |
At a glance
- No Expedited review granted
- No Approval order on file
- No Summary of safety and effectiveness on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA supplements
A PMA supplement asks FDA to approve a change to a device that already holds a premarket approval: a new indication, a design or labeling change, a manufacturing site or process change.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: