Product code GWI— Neurology
AESTHESIOMETER
- Classification name
- Discriminator, Two-Point
- Device class
- Class 1
- Regulation
- 21 CFR 882.1200
- Advisory panel
- Neurology
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code GWI
FDA has cleared devices under product code GWI between 1987 and 1995, filed by 2 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
- 1995
- 1987
Top applicants under product code GWI
Recent clearances under product code GWI
Data sourced from openFDA. This site is unofficial and independent of the FDA.