DeviceClearance

Product code CAX— Anesthesiology

AIRCO 2000 SERIES FLOWMETERS

Classification name
Flowmeter, Tube, Thorpe, Back-Pressure Compensated
Device class
Class 1
Regulation
21 CFR 868.2340
Advisory panel
Anesthesiology
Total cleared
24
First cleared
Most recent

Market context for product code CAX

FDA has cleared 24 devices under product code CAX between 1976 and 1993, filed by 16 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 CAX

Adverse events under product code CAX

product code CAX
Death
3
Other
1
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 CAX

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