The association supports reclassifying ECT devices as medium risk, which would preclude the need for additional research regarding their safety and effectiveness.
On Friday, a majority of experts on the panel expressed support for classifying ECT devices as high risk for the treatment of depression and several other conditions.
For decades psychiatrists have used shock therapy to treat cases of depression that haven't been helped by antidepressant medications, and in recent years the treatment -- now known as electroconvulsive therapy (ECT) -- has experienced something of a revival.
If the FDA follows the panel's advice, as it usually does, the makers of ECT devices may need to provide the agency with additional safety and efficacy evidence, like that required for prescription drugs.
On the other side, patients' rights organizations and advocacy groups such as the Depression and Bipolar Support Alliance (DBSA) have urged the FDA not to hastily reclassify ECT devices.