Product code KCR— Dental
FACEBOW FOR BALANCE ARTICULATOR
- Classification name
- Facebow
- Device class
- Class 1
- Regulation
- 21 CFR 872.3220
- Advisory panel
- Dental
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code KCR
FDA has cleared device under product code KCR, all in 1983, filed by 1 applicant company. 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.
Top applicants under product code KCR
Recent clearances under product code KCR
Data sourced from openFDA. This site is unofficial and independent of the FDA.