Product code JAM— Radiology
CLEON IMAGER
- Classification name
- Scanner, Whole Body, Nuclear
- Device class
- Class 1
- Regulation
- 21 CFR 892.1330
- Advisory panel
- Radiology
- Total cleared
- 3
- First cleared
- Most recent
Market context for product code JAM
FDA has cleared devices under product code JAM between 1977 and 1984, 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
- 1984
- 1977
Top applicants under product code JAM
Recent clearances under product code JAM
Data sourced from openFDA. This site is unofficial and independent of the FDA.