LQW — Test, Temperature Discrimination Class I
FDA Device Classification
Classification Details
- Product Code
- LQW
- Device Class
- Class I
- Regulation Number
- 882.1200
- Submission Type
- Review Panel
- NE
- Medical Specialty
- Neurology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K141208 | prosenex | DYNAMIC NEUROSCREENING DEVICE | July 23, 2014 |
| K922052 | medoc | TSA 2001 THERMAL SENSORY ANALYZER | October 21, 1993 |
| K864345 | sensortek | NTE-2 THERMAL SENSITIVITY TESTER | January 29, 1987 |