DeviceClearance

Product code BYX— Anesthesiology

OXYCOIL

Classification name
Tubing, Pressure And Accessories
Device class
Class 1
Regulation
21 CFR 868.5860
Advisory panel
Anesthesiology
Total cleared
62
First cleared
Most recent

Market context for product code BYX

FDA has cleared 62 devices under product code BYX between 1976 and 2001, 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 BYX

Recent clearances under product code BYX

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