Product code CBG— Anesthesiology
SOFT EAR STETHOSCOPE
- Classification name
- Spreader, Cuff
- Device class
- Class 1
- Regulation
- 21 CFR 868.5760
- Advisory panel
- Anesthesiology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code CBG
FDA has cleared device under product code CBG, all in 1987, 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 CBG
Recent clearances under product code CBG
Data sourced from openFDA. This site is unofficial and independent of the FDA.