Product code BYW— Anesthesiology
HYPEX
- Classification name
- Device, Rebreathing
- Device class
- Class 1
- Regulation
- 21 CFR 868.5675
- Advisory panel
- Anesthesiology
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code BYW
FDA has cleared devices under product code BYW between 1980 and 1990, 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
- 1990
- 1980
Top applicants under product code BYW
Recent clearances under product code BYW
Data sourced from openFDA. This site is unofficial and independent of the FDA.