Catheter, Percutaneous

What Is FDA Product Code DQY?

Catheter, Percutaneous is FDA product code DQY, Class 2, 21 CFR 870.1250.

How Does It Reach the US Market?

A 510(k) premarket notification is required before it is sold in the United States: the applicant shows the device is substantially equivalent to one already on the market. The review can be done by an FDA-accredited third party, which is usually faster. Chinese applicants hold 5 clearances under this code; the FDA took a median of 192 days from receipt to decision on them.

What Do the Recalls Say?

The FDA has recorded 620 recalls under this product code since 2002. None was by a company in China. 220 are Class I, the most serious grade.

The root causes the FDA records most often are Component design/selection (216), Process control (45) and Employee error (38). A recall is a fact about one product and its maker, not a grade for every manufacturer of the type.