Product code BXL— Anesthesiology
MINI OX III OXYGEN MONITOR
- Classification name
- Algesimeter, Manual
- Device class
- Class 1
- Regulation
- 21 CFR 868.1030
- Advisory panel
- Anesthesiology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code BXL
FDA has cleared device under product code BXL, all in 1983, 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 BXL
Recent clearances under product code BXL
Data sourced from openFDA. This site is unofficial and independent of the FDA.