Product code KCA— Ear, Nose, Throat
MACKENZIE'S TONSILLECTOME
- Classification name
- Tonsillectome
- 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 KCA
FDA has cleared device under product code KCA, all in 1982, 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 KCA
Recent clearances under product code KCA
Data sourced from openFDA. This site is unofficial and independent of the FDA.