DeviceClearance

Product code CAI— Anesthesiology

ANESTHESIA BREATHING CIRCUIT

Classification name
Circuit, Breathing (W Connector, Adaptor, Y Piece)
Device class
Class 1
Regulation
21 CFR 868.5240
Advisory panel
Anesthesiology
Total cleared
184
First cleared
Most recent

Market context for product code CAI

FDA has cleared 184 devices under product code CAI between 1976 and 1995, filed by 84 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 CAI

Adverse events under product code CAI

product code CAI
Malfunction
869
Other
1
Total
870

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 CAI

1–100 of 184

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