Product code CAD— Anesthesiology

DRAGER-VAPOR 19.1 W/PLUG SYSTEM S PLUS

Classification name
Vaporizer, Anesthesia, Non-Heated
Device class
Class 2
Regulation
21 CFR 868.5880
Advisory panel
Anesthesiology
Total cleared
57
First cleared
Most recent

Market context for product code CAD

FDA has cleared 57 devices under product code CAD between 1976 and 2024, filed by 31 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

last 15 years

Top applicants under product code CAD

Adverse events under product code CAD

product code CAD
Malfunction
3,275
Total
3,275

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 CAD

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