DeviceClearance

Product code DWF— Cardiovascular

AngioVac Cannula

Classification name
Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
Device class
Class 2
Regulation
21 CFR 870.4210
Advisory panel
Cardiovascular
Total cleared
401
First cleared
Most recent

Market context for product code DWF

FDA has cleared 401 devices under product code DWF between 1977 and 2026, filed by 120 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 DWF

Adverse events under product code DWF

product code DWF
Death
106
Injury
386
Malfunction
2,323
Total
2,815

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 DWF

1–100 of 401

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