Product code KCB— Ear, Nose, Throat
FRAZIER-FERGUSON SUCTION TUBES
- Classification name
- Tube, Tonsil Suction
- Device class
- Class 1
- Regulation
- 21 CFR 874.4420
- Advisory panel
- Ear, Nose, Throat
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code KCB
FDA has cleared device under product code KCB, all in 1980, 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 KCB
Recent clearances under product code KCB
Data sourced from openFDA. This site is unofficial and independent of the FDA.