Zdrowie i gospodarka · 04/06/1997
FDA Orders Manufacturers of Cranial Electrotherapy Stimulators to Submit Safety and Effectiveness Information
The FDA is requiring manufacturers of cranial electrotherapy stimulators to submit information on the device's safety and effectiveness, which may lead to a revision of its classification or the issuance of a premarket approval application requirement.
Source: Federal Register — Food and Drug AdministrationOpen original release →