DeviceClearance

Product code DQY— Cardiovascular

VISTA BRITE TIP CATHETERS

Classification name
Catheter, Percutaneous
Device class
Class 2
Regulation
21 CFR 870.1250
Advisory panel
Cardiovascular
Total cleared
895
First cleared
Most recent

Market context for product code DQY

FDA has cleared 895 devices under product code DQY between 1979 and 2026, filed by 278 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 DQY

Adverse events under product code DQY

product code DQY
Death
464
Injury
4,489
Malfunction
13,721
Other
2
Total
18,676

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 DQY

1–100 of 895

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