DeviceClearance

Product code ECX— Anesthesiology

Intelli-Ox

Classification name
Cylinder, Compressed Gas, And Valve
Device class
Class 1
Regulation
21 CFR 868.2700
Advisory panel
Anesthesiology
Total cleared
13
First cleared
Most recent

Market context for product code ECX

FDA has cleared 13 devices under product code ECX between 1977 and 2017, filed by 12 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

Top applicants under product code ECX

Recent clearances under product code ECX

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