DeviceClearance

Product code DQO— Cardiovascular

Arterial Pressure Monitoring Set/Tray

Classification name
Catheter, Intravascular, Diagnostic
Device class
Class 2
Regulation
21 CFR 870.1200
Advisory panel
Cardiovascular
Total cleared
501
First cleared
Most recent

Market context for product code DQO

FDA has cleared 501 devices under product code DQO between 1976 and 2026, filed by 204 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 DQO

Adverse events under product code DQO

product code DQO
Death
35
Injury
993
Malfunction
1,772
Other
5
Total
2,805

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 DQO

1–100 of 501

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