Product code BYO— Anesthesiology
2C7125 BLOW BOTTLE
- Classification name
- Bottle, Blow
- Device class
- Class 1
- Regulation
- 21 CFR 868.5220
- Advisory panel
- Anesthesiology
- Total cleared
- 4
- First cleared
- Most recent
Market context for product code BYO
FDA has cleared devices under product code BYO between 1978 and 1993, 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
- 1993
- 1992
- 1978
Top applicants under product code BYO
Recent clearances under product code BYO
Data sourced from openFDA. This site is unofficial and independent of the FDA.