Product code KFE— Hematology
NEUTRAL RED
- Classification name
- Neutral Red
- Device class
- Class 1
- Regulation
- 21 CFR 864.1850
- Advisory panel
- Hematology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code KFE
FDA has cleared device under product code KFE, 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 KFE
Recent clearances under product code KFE
Data sourced from openFDA. This site is unofficial and independent of the FDA.