Product code KAP— Ear, Nose, Throat
CURETTE SET, ANTRUM, COAKLEY
- Classification name
- Curette, Nasal
- 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 KAP
FDA has cleared device under product code KAP, all in 1987, 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 KAP
Recent clearances under product code KAP
Data sourced from openFDA. This site is unofficial and independent of the FDA.