PMA supplement
P830037 S034: DURASOFT R3 (PHEMFILCON A) LENSES
FDA PMA supplement · Normal 180 Day Track · Alcon Laboratories, Inc.
Key facts
| Original PMA | P830037 |
|---|---|
| Supplement number | S034 |
| Supplement type | Normal 180 Day Track |
| Reason for the supplement | Location Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | DURASOFT R3 (PHEMFILCON A) LENSES |
| Generic name | Lenses, soft contact, extended wear |
| Applicant | Alcon Laboratories, Inc. |
| Product code | LPM |
| Received date | Feb 26, 1993 |
| Decision date | Jan 31, 1994 |
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: