Device recall
Z-0470-2007: International Technidyne Corporation (ITC) ProTime Microcoagulation System…
FDA device recall · Class III · International Technidyne Corp.
Key facts
| Recall number (Z-number) | Z-0470-2007 |
|---|---|
| Recall event | 36956 |
| Product | International Technidyne Corporation (ITC) ProTime Microcoagulation System Instrument-Catalogue Number-Protimeint & Protimepro, Protimeintrf & Protimeprorf, Protimeintl & Protimeprol. |
| Product code | GJS |
| Recalling firm | International Technidyne Corp. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 26, 2007 |
| 510(k) numbers | K951072 |
| FEI number | 1000526865 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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