Product code JRR— Clinical Chemistry
AQUAMATIC K-MODULE MODEL K-10
- Classification name
- Regulator, Temperature
- Device class
- Class 1
- Regulation
- 21 CFR 862.2050
- Advisory panel
- Clinical Chemistry
- Total cleared
- 4
- First cleared
- Most recent
Market context for product code JRR
FDA has cleared devices under product code JRR between 1977 and 1982, filed by 4 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
- 1982
- 1980
- 1978
- 1977
Top applicants under product code JRR
Recent clearances under product code JRR
Data sourced from openFDA. This site is unofficial and independent of the FDA.