Product code KCM— Ear, Nose, Throat
POST-AID
- Classification name
- Dropper, Ent
- Device class
- Class 1
- Regulation
- 21 CFR 874.5220
- Advisory panel
- Ear, Nose, Throat
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code KCM
FDA has cleared device under product code KCM, all in 1984, 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 KCM
Recent clearances under product code KCM
Data sourced from openFDA. This site is unofficial and independent of the FDA.