Cystometer, Electrical Recording

How Is EXQ Classified?

Cystometer, Electrical Recording is FDA product code EXQ, Class 2, 21 CFR 876.1620.

How Does It Reach the US Market?

It is exempt from premarket notification: the manufacturer registers its establishment and lists the device, and no 510(k) is needed before it is sold in the United States.

What Has Gone Wrong With It?

The FDA has recorded 1 recall under this product code since 2009. None was by a company in China. The root cause the FDA records most often is Packaging process control (1).

A recall is a fact about one product and its maker, not a grade for every manufacturer of the type.