Product code FEJ— Gastroenterology, Urology
TBI TRAINER
- Classification name
- Attachment, Binocular, For Endoscope
- Device class
- Class 1
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code FEJ
FDA has cleared device under product code FEJ, all in 1985, 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 FEJ
Recent clearances under product code FEJ
Data sourced from openFDA. This site is unofficial and independent of the FDA.