PMA supplement
P990021 S001: DIOMED 630 PDT LASER
FDA PMA supplement · Panel Track · Pinnacle Biologics, Inc.
Key facts
| Original PMA | P990021 |
|---|---|
| Supplement number | S001 |
| Supplement type | Panel Track |
| Reason for the supplement | Labeling Change - Indications/instructions/shelf life/tradename |
| Trade name | DIOMED 630 PDT LASER |
| Generic name | System, laser, photodynamic therapy |
| Applicant | Pinnacle Biologics, Inc. |
| Product code | MVF |
| Received date | Jun 12, 2002 |
| Decision date | Aug 1, 2003 |
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: