PMA supplement
P860003 S095: CELLEX PHOTOPHERESIS SYSTEM
FDA PMA supplement · 30-Day Notice · Therakos Development Limited
Key facts
| Original PMA | P860003 |
|---|---|
| Supplement number | S095 |
| Supplement type | 30-Day Notice |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | CELLEX PHOTOPHERESIS SYSTEM |
| Generic name | System, photopheresis, extracorporeal |
| Applicant | Therakos Development Limited |
| Product code | LNR |
| Received date | Aug 16, 2017 |
| Decision date | Sep 14, 2017 |
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: