Product code KBD— Ear, Nose, Throat
13-320,13-330 TWO TYPES NAZAL SCISSORS-HEYMAN,BECK
- Classification name
- Scissors, Nasal
- Device class
- Class 1
- Regulation
- 21 CFR 874.4420
- Advisory panel
- Ear, Nose, Throat
- Total cleared
- 3
- First cleared
- Most recent
Market context for product code KBD
FDA has cleared devices under product code KBD between 1979 and 1985, filed by 3 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
- 1985
- 1982
- 1979
Top applicants under product code KBD
Recent clearances under product code KBD
Data sourced from openFDA. This site is unofficial and independent of the FDA.