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<oembed><version>1.0</version><provider_name>CLP Blog</provider_name><provider_url>https://clpblog.citizen.org</provider_url><author_name>Brian Wolfman</author_name><title>"The FDA is still letting doctors implant untested devices into our bodies" - CLP Blog</title><type>rich</type><width>600</width><height>338</height><html>&lt;blockquote class="wp-embedded-content" data-secret="jhm4OUb7WL"&gt;&lt;a href="https://clpblog.citizen.org/the-fda-is-still-letting-doctors-implant-untested-devices-into-our-bodies/"&gt;&#x201C;The FDA is still letting doctors implant untested devices into our bodies&#x201D;&lt;/a&gt;&lt;/blockquote&gt;&lt;iframe sandbox="allow-scripts" security="restricted" src="https://clpblog.citizen.org/the-fda-is-still-letting-doctors-implant-untested-devices-into-our-bodies/embed/#?secret=jhm4OUb7WL" width="600" height="338" title="&#x201C;&#x201C;The FDA is still letting doctors implant untested devices into our bodies&#x201D;&#x201D; &#x2014; CLP Blog" data-secret="jhm4OUb7WL" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"&gt;&lt;/iframe&gt;&lt;script type="text/javascript"&gt;
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</html><description>That's the name of this Washington Post article by Jeanne Lenzer and Shannon Brownlee. The article explains that the FDA continues to allow critical, implanted medical devices on the market via the so-called "510(k) process." Among other serious deficiencies, the 510(k) process does not require pre-market clinical safety testing. Lenzer and Brownlee explain that the [...]</description></oembed>
