Device recall
Z-2121-2016: The ZYTO Select and ZYTO Elite software programs are used to rank pairs of…
FDA device recall · Class II · ZYTO Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-2121-2016 |
|---|---|
| Recall event | 74273 |
| Product | The ZYTO Select and ZYTO Elite software programs are used to rank pairs of galvanic skin response measurements from most coherent (the second scan is closest in time measurement to the baseline original scan) to least coherent (further away from the baseline). |
| Product code | GZO |
| Recalling firm | ZYTO Technologies, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 21, 2017 |
| 510(k) numbers | K111308 |
| FEI number | 3008493238 |
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