Product code KJG— Pathology
24 CELL WELLS TISSUE CULTURE
- Classification name
- Tube, Tissue Culture
- Device class
- Class 1
- Regulation
- 21 CFR 864.3010
- Advisory panel
- Pathology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code KJG
FDA has cleared device under product code KJG, all in 1983, 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 KJG
Recent clearances under product code KJG
Data sourced from openFDA. This site is unofficial and independent of the FDA.