QiG Group LLC
3 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Algostim LLC, Algovita Implanted Pulse Generator stimulator, Model 2408 ( 3 x 8 channel) recall (Z-1192-2016) | QiG Group LLC | 2016-03-18 |
| Algostim LLC, Algovita Implanted Pulse Generator stimulator, Model 2412 ( 2 x 12 channel) recall (Z-1193-2016) | QiG Group LLC | 2016-03-18 |
| Algostim LLC, Algovita External Pulse Generator, Trial Stimulator, Model 3400 recall (Z-1194-2016) | QiG Group LLC | 2016-03-18 |
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Every clearance here is in the API, with alerts when new ones post.