Product code CFA— Clinical Chemistry
MAGNESIUM PROCEDURE
- Classification name
- Electrode, Ion Specific, Magnesium
- Device class
- Class 1
- Regulation
- 21 CFR 862.1495
- Advisory panel
- Clinical Chemistry
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code CFA
FDA has cleared devices under product code CFA between 1985 and 1986, filed by 2 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
- 1986
- 1985
Top applicants under product code CFA
Recent clearances under product code CFA
Data sourced from openFDA. This site is unofficial and independent of the FDA.