PMA supplement
N18180 S003: CUSTOMFLEX (DELTAFILCON A) HYDROPHILIC CONTACT LEN
FDA PMA supplement · Wesley Jessen Corp.
Key facts
| Original PMA | N18180 |
|---|---|
| Supplement number | S003 |
| Trade name | CUSTOMFLEX (DELTAFILCON A) HYDROPHILIC CONTACT LEN |
| Generic name | Lenses, soft contact, daily wear |
| Applicant | Wesley Jessen Corp. |
| Product code | LPL |
| Received date | Jan 19, 1981 |
| Decision date | May 11, 1981 |
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: