Product code FEI— Gastroenterology, Urology
FLEXIBLE VISUALIZATION CATHETER
- Classification name
- Instrument, Special Lens, For Endoscope
- Device class
- Class 1
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code FEI
FDA has cleared devices under product code FEI between 1986 and 1988, 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
- 1988
- 1986
Top applicants under product code FEI
Recent clearances under product code FEI
Data sourced from openFDA. This site is unofficial and independent of the FDA.