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AEMD > SEC Filings for AEMD > Form 8-K on 25-Jun-2013All Recent SEC Filings

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Form 8-K for AETHLON MEDICAL INC


25-Jun-2013

Other Events


Item 8.01 Other Events.

On June 20, 2013, the United States Food and Drug Administration (FDA) approved an Investigational Device Exemption that allows the Registrant to initiate human feasibility studies of the Aethlon Hemopurifier® in the United States. .

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