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Read now - Mental Health Association of Maryland
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proposed administrative order to reclassify the ECT device for ...
Electroshock Devices Will Never Have To Prove Safe Or Effective ...
7 Mar 2016 ... ECT sends an electrical shock into a person\'s brain in
order to ... The FDA is now
attempting to reclassify ECT machines as less dangerous Class II devices, a
class ... To send a comment to the FDA, click here. ... Electroshock Devices Will
Never Have To Prove Safe Or Effective Under Proposed FDA Rule ...
News: Today, Friday, is Deadline for You to Speak Out Against ...
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oppose the FDA\'s
proposed reclassification of the ECT device to Class II. ... Pre-
Market Approval (PMA) process in order to establish their safety and
effectiveness.
FDA To Allow Electroshock Therapy - Infinite Unknown
14 Mar 2016 ... Global News, Health, Politics Add comments. – FDA to declassify electroshock therapy to same risk category as condoms and contact lenses: ... the reclassification process for Electroconvulsive Therapy Devices (ECT) in early
January. ... “The proposal has reignited a firestorm that the FDA has colluded ...
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23 Dec 2009 ... ... classification process for this device pertains to the ``Order for Certain Class III
... considering whether to issue a
proposed rule requiring the device to ... classification of ECT devices will be subject to notice and comment
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The FDA is issuing a
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depressive episode ...
Max Fink writes to the FDA - ECT.org
... FDA
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class ... international experience since 1934, and numerous recent expert reviews, ... in mania, and the recommendations for a sequence in treatment
parameters.
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