Product code KJC— Hematology
IN VITRO 2.5X ROLLER BOTTLE
- Classification name
- Bottle, Roller, Tissue Culture
- Device class
- Class 1
- Regulation
- 21 CFR 864.2240
- Advisory panel
- Hematology
- Total cleared
- 3
- First cleared
- Most recent
Market context for product code KJC
FDA has cleared devices under product code KJC between 1979 and 1988, filed by 3 applicant companies. 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.
Clearances per year
- 1988
- 1987
- 1979
Top applicants under product code KJC
Recent clearances under product code KJC
Data sourced from openFDA. This site is unofficial and independent of the FDA.