Product code KYS— General Hospital
FUNGUS FIGHTER INSOLES
- Classification name
- Insoles, Medical
- Device class
- Class 1
- Regulation
- 21 CFR 880.6280
- Advisory panel
- General Hospital
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code KYS
FDA has cleared device under product code KYS, 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 KYS
Recent clearances under product code KYS
Data sourced from openFDA. This site is unofficial and independent of the FDA.