DeviceClearance

Product code BZB— Anesthesiology

OXYGEN CATHETERS

Classification name
Catheter, Nasal, Oxygen
Device class
Class 1
Regulation
21 CFR 868.5350
Advisory panel
Anesthesiology
Total cleared
8
First cleared
Most recent

Market context for product code BZB

FDA has cleared 8 devices under product code BZB between 1979 and 1990, filed by 8 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 BZB

Recent clearances under product code BZB

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