Cranial Electrotherapy Stimulator to Treat Insomnia And/Or Anxiety

What Is It?

To provide electrical current to the head to treat insomnia and/or anxiety

What Is FDA Product Code QJQ?

Cranial Electrotherapy Stimulator To Treat Insomnia And/Or Anxiety is FDA product code QJQ, Class 2, 21 CFR 882.5800.

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. No clearance under this code names a Chinese applicant. A registration is not a clearance: the plants above are set up to make it, and the 510(k) it is sold under is held by whoever files it, often the brand.

What Has Gone Wrong With It?

The FDA has recorded 1 recall under this product code since 2023. None was by a company in China. The root cause the FDA records most often is Nonconforming Material/Component (1).

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