Device recall
Z-0578-05: Dermosonic Model 430300 and 440100 Non-Invasive Subdermal Therapy System
FDA device recall · Class II · Sybaritic, Inc
Key facts
| Recall number (Z-number) | Z-0578-05 |
|---|---|
| Recall event | 30792 |
| Product | Dermosonic Model 430300 and 440100 Non-Invasive Subdermal Therapy System |
| Product code | IMI |
| Recalling firm | Sybaritic, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 7, 2007 |
| 510(k) numbers | K024307 |
| FEI number | 2131125 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database