Product code FFF— Gastroenterology, Urology
EXTENDED COVERS, STERILE
- Classification name
- Cover, Biopsy Forceps
- Device class
- Class 1
- Regulation
- 21 CFR 876.1075
- Advisory panel
- Gastroenterology, Urology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code FFF
FDA has cleared device under product code FFF, all in 1989, 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 FFF
Recent clearances under product code FFF
Data sourced from openFDA. This site is unofficial and independent of the FDA.