PMA supplement
P830006 S006: SOFTACT II (POLYMACON)
FDA PMA supplement · Normal 180 Day Track · Premier Contact Lens
Key facts
| Original PMA | P830006 |
|---|---|
| Supplement number | S006 |
| Supplement type | Normal 180 Day Track |
| Reason for the supplement | Location Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | SOFTACT II (POLYMACON) |
| Generic name | Lenses, soft contact, daily wear |
| Applicant | Premier Contact Lens |
| Product code | LPL |
| Received date | Feb 18, 1992 |
| Decision date | Apr 15, 1992 |
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: