PMA supplement
P830034 S030: ALCON MULTI-PURPOSE SOLUTION ID 81573
FDA PMA supplement · Normal 180 Day Track · Alcon Laboratories
Key facts
| Original PMA | P830034 |
|---|---|
| Supplement number | S030 |
| Supplement type | Normal 180 Day Track |
| Reason for the supplement | Change Design/Components/Specifications/Material |
| Trade name | ALCON MULTI-PURPOSE SOLUTION ID 81573 |
| Generic name | Accessories, soft lens products |
| Applicant | Alcon Laboratories |
| Product code | LPN |
| Received date | Aug 20, 1996 |
| Decision date | Feb 10, 1997 |
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: