Product code KBM— Ear, Nose, Throat
TONSIL SPONGE, GAUZE DISSECTOR, CYLINDRICAL SPONGES
- Classification name
- Dissector, Tonsil
- 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 KBM
FDA has cleared device under product code KBM, all in 1994, 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 KBM
Recent clearances under product code KBM
Data sourced from openFDA. This site is unofficial and independent of the FDA.