Product code LQW— Neurology
DYNAMIC NEUROSCREENING DEVICE
- Classification name
- Test, Temperature Discrimination
- Device class
- Class 1
- Regulation
- 21 CFR 882.1200
- Advisory panel
- Neurology
- Total cleared
- 3
- First cleared
- Most recent
Market context for product code LQW
FDA has cleared devices under product code LQW between 1987 and 2014, filed by 3 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 2014
- 1993
- 1987
Top applicants under product code LQW
Recent clearances under product code LQW
Data sourced from openFDA. This site is unofficial and independent of the FDA.