DeviceClearance

Product code BYD— Anesthesiology

FLOCARE

Classification name
Condenser, Heat And Moisture (Artificial Nose)
Device class
Class 1
Regulation
21 CFR 868.5375
Advisory panel
Anesthesiology
Total cleared
73
First cleared
Most recent

Market context for product code BYD

FDA has cleared 73 devices under product code BYD between 1979 and 1996, filed by 33 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

last 15 years

Top applicants under product code BYD

Recent clearances under product code BYD

Data sourced from openFDA. This site is unofficial and independent of the FDA.