DeviceClearance

Product code CBH— Anesthesiology

ENDOTRACHEAL TUBE HOLDER

Classification name
Device, Fixation, Tracheal Tube
Device class
Class 1
Regulation
21 CFR 868.5770
Advisory panel
Anesthesiology
Total cleared
47
First cleared
Most recent

Market context for product code CBH

FDA has cleared 47 devices under product code CBH between 1978 and 2014, 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 CBH

Adverse events under product code CBH

product code CBH
Death
7
Total
7

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recent clearances under product code CBH

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