FDA Product Code
FDA Product Code LQW — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Neurology
- 21 CFR Citation
- 882.1200
510(k) Clearances — 3 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K141208 | DYNAMIC NEUROSCREENING DEVICE | Prosenex | 2014-07-23 | Traditional | PDF ↗ |
| K922052 | TSA 2001 THERMAL SENSORY ANALYZER | Medoc Corp. | 1993-10-21 | Traditional | PDF ↗ |
| K864345 | NTE-2 THERMAL SENSITIVITY TESTER | Sensortek, Inc. | 1987-01-29 | Traditional | PDF ↗ |
Product code LQW · Class I · Neurology. Data: openFDA.