PMA supplement
P820051 S002: OCU-FLEX
FDA PMA supplement · Ocu-Ease Optical Products, Inc.
Key facts
| Original PMA | P820051 |
|---|---|
| Supplement number | S002 |
| Trade name | OCU-FLEX |
| Generic name | Lenses, soft contact, daily wear |
| Applicant | Ocu-Ease Optical Products, Inc. |
| Product code | LPL |
| Received date | Aug 5, 1985 |
| Decision date | Feb 20, 1986 |
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: