Product code IXO— Radiology
POST EXTRA SYSTOLIC POSTENTLATOR
- Classification name
- Synchronizer, Ecg / Respirator, Radiographic
- Device class
- Class 1
- Regulation
- 21 CFR 892.1970
- Advisory panel
- Radiology
- Total cleared
- 4
- First cleared
- Most recent
Market context for product code IXO
FDA has cleared devices under product code IXO between 1980 and 1986, 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
- 1986
- 1981
- 1980
Top applicants under product code IXO
Recent clearances under product code IXO
Data sourced from openFDA. This site is unofficial and independent of the FDA.