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January 28, 2011 The U.S. Food and Drug Administration (FDA) advisory panel met on January 27 and 28th to discuss lowering the devices used for electroconvulsive therapy (ECT) from Class III devices to Class II devices. The advisory panel considered clinical studies and public comments on reclassifying the devices. Download the Report . . .

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Market Intelligence Resource | January 28, 2011

FDA Executive Summary: Neurological Devices Panel Meeting to Discuss the Classification of Electroconvulsive Therapy Devices

January 28, 2011 The U.S. Food and Drug Administration (FDA) advisory panel met on January 27 and 28th to discuss lowering the devices used for electroconvulsive therapy (ECT) from Class III devices to Class II devices. The advisory panel considered clinical studies and public comments on reclassifying the devices. Download the Report . . .

Want To Read More? Log In Or Become A Paid Member
Resource Available For Paid OPEN MINDS Circle Members Only
Not a paid member? Don't miss out! Sign up today and receive unlimited organizational access to all OPEN MINDS strategic advice, market intelligence, and management best practices – over 250,000 resources!
Log In
If you are already a paid member, log in to your account to access this resource and more. If you are a free member, you will need to upgrade to a paid membership before accessing this resource.

Become A Paid Member
If you are not yet a paid member, learn more about the OPEN MINDS Circle Market Intelligence Service Membership on our website, reach out to our team at info@openminds.com, or call us at 877-350-6463.