DeviceClearance

Product code CAE— Anesthesiology

AIRWAYS

Classification name
Airway, Oropharyngeal, Anesthesiology
Device class
Class 1
Regulation
21 CFR 868.5110
Advisory panel
Anesthesiology
Total cleared
57
First cleared
Most recent

Market context for product code CAE

FDA has cleared 57 devices under product code CAE between 1976 and 2014, filed by 51 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 CAE

Adverse events under product code CAE

product code CAE
Death
4
Total
4

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 CAE

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