LQW
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Test, Temperature Discrimination
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 882.1200
- Medical specialty
- Neurology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| DYNAMIC NEUROSCREENING DEVICE (K141208) | Prosenex | 2014-07-23 |
| TSA 2001 THERMAL SENSORY ANALYZER (K922052) | Medoc Corp. | 1993-10-21 |
| NTE-2 THERMAL SENSITIVITY TESTER (K864345) | Sensortek, Inc. | 1987-01-29 |
Track LQW automatically
Every clearance here is in the API, with alerts when new ones post.