Product code KFD— Hematology
MODIFIED POLYCHROME IV STAIN
- Classification name
- Aniline Blue
- Device class
- Class 1
- Regulation
- 21 CFR 864.1850
- Advisory panel
- Hematology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code KFD
FDA has cleared device under product code KFD, all in 1989, 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 KFD
Recent clearances under product code KFD
Data sourced from openFDA. This site is unofficial and independent of the FDA.