Product code KAS— Ear, Nose, Throat
WOUND SPAN BRIDGE III
- Classification name
- Knife, 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 KAS
FDA has cleared device under product code KAS, all in 1978, 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 KAS
Recent clearances under product code KAS
Data sourced from openFDA. This site is unofficial and independent of the FDA.