Has the Food and Drug Administration (FDA) classified the AIT devices as harmful?
No, the FDA has not classified AIT devices as harmful. Any device for which there are claims that it will improve or cure a condition is automatically labeled a `medical device’ by the FDA. Recently, the FDA clarified their position regarding AIT devices. That is, as long as AIT devices are not promoted as ‘medical devices,’ then the FDA does not have jurisdiction over them.
