Federal Register: Electroconvulsive Therapy Devices for Class II Intended Uses: Draft Guidance for Industry, Clinicians, and FDA Staff; Availability

The FDA is announcing the availability of the draft guidance ``Electroconvulsive Therapy (ECT) Devices for Class II Intended Uses: Draft Guidance for Industry, Clinicians, and FDA Staff.'' The purpose of this guidance is to make recommendations for 510...
Source: Food and Drug Adminstration (FDA): CDRHNew - Category: Medical Equipment Source Type: news