Product code JRA— Clinical Chemistry
GENESIS RMP
- Classification name
- Microtitrator, For Clinical Use
- Device class
- Class 1
- Regulation
- 21 CFR 862.2680
- Advisory panel
- Clinical Chemistry
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code JRA
FDA has cleared device under product code JRA, all in 1997, 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 JRA
Recent clearances under product code JRA
Data sourced from openFDA. This site is unofficial and independent of the FDA.