Product code KIY— Hematology
TEST SYSTEM TISSUE CELL CULTURE SLIDE
- Classification name
- Chamber, Slide Culture
- Device class
- Class 1
- Regulation
- 21 CFR 864.2240
- Advisory panel
- Hematology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code KIY
FDA has cleared device under product code KIY, 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 KIY
Recent clearances under product code KIY
Data sourced from openFDA. This site is unofficial and independent of the FDA.