GZP
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Stimulator, Mechanical, Evoked Response
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 882.1880
- Medical specialty
- Neurology
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| EyeStat (K191700) | Blinktbi, Inc. | 2019-12-09 |
| SOMATOSENSORY STIMULUS SYSTEM (K913604) | Biomagnetic Technologies, Inc. | 1991-12-09 |
Track GZP automatically
Every clearance here is in the API, with alerts when new ones post.