The US Food & Drug Administration holds a meeting about electroshock device
Info The US FDA announced that on January 27 and 28, 2011, a US Food & Drug Administration committee will “discuss and make recommendations regarding the possible reclassification of devices indicated for use in electroconvulsive therapy.” What Forum When Jan 27, 2011 08:00 AM to Jan 28, 2011 06:00 PM Where Gaithersburg, MD Contact Name…