DeviceClearance

Product code BYH— Anesthesiology

MOISTURE TRAP

Classification name
Drain, Tee (Water Trap)
Device class
Class 1
Regulation
21 CFR 868.5995
Advisory panel
Anesthesiology
Total cleared
22
First cleared
Most recent

Market context for product code BYH

FDA has cleared 22 devices under product code BYH between 1977 and 1995, filed by 13 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 BYH

Recent clearances under product code BYH

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