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	Comments for FDA 510(k) Consulting Service for Medical Devices	</title>
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		Comment on FDA 510(k) Clearance Consulting for Medical Devices and IVD&#8217;s by ISOplan USA		</title>
		<link>http://www.fda-510k.com/fda-510k-clearance-consulting-for-medical-devices-and-ivds/comment-page-1/#comment-71</link>

		<dc:creator><![CDATA[ISOplan USA]]></dc:creator>
		<pubDate>Wed, 25 Jul 2018 16:01:29 +0000</pubDate>
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					<description><![CDATA[In reply to &lt;a href=&quot;http://www.fda-510k.com/fda-510k-clearance-consulting-for-medical-devices-and-ivds/comment-page-1/#comment-70&quot;&gt;Kristen Lapina&lt;/a&gt;.

Thank you for contacting ISOplan.

Please let us know how we can assist you.

Kind regards,

Lorenzo Da Madice
...................................................................
ISOplan USA
1368 North US 1 - Suite 402
Ormond Beach, FL 32174 (USA)
Phone  386-868-0618
http://www.fda-510k.com]]></description>
			<content:encoded><![CDATA[<p>In reply to <a href="http://www.fda-510k.com/fda-510k-clearance-consulting-for-medical-devices-and-ivds/comment-page-1/#comment-70">Kristen Lapina</a>.</p>
<p>Thank you for contacting ISOplan.</p>
<p>Please let us know how we can assist you.</p>
<p>Kind regards,</p>
<p>Lorenzo Da Madice<br />
&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;.<br />
ISOplan USA<br />
1368 North US 1 &#8211; Suite 402<br />
Ormond Beach, FL 32174 (USA)<br />
Phone  386-868-0618<br />
<a href="http://www.fda-510k.com" rel="ugc">http://www.fda-510k.com</a></p>
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		Comment on FDA 510(k) Clearance Consulting for Medical Devices and IVD&#8217;s by Kristen Lapina		</title>
		<link>http://www.fda-510k.com/fda-510k-clearance-consulting-for-medical-devices-and-ivds/comment-page-1/#comment-70</link>

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		<pubDate>Wed, 25 Jul 2018 11:03:05 +0000</pubDate>
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					<description><![CDATA[Hi,  We are in need of  FDA Consultant with experience and compliance in Medical Instruments

Thanks]]></description>
			<content:encoded><![CDATA[<p>Hi,  We are in need of  FDA Consultant with experience and compliance in Medical Instruments</p>
<p>Thanks</p>
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		Comment on FDA Regulations by FDA 510(k) Premarket Notification Process		</title>
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		<pubDate>Tue, 28 May 2013 09:34:05 +0000</pubDate>
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		Comment on FDA 510(k) Process by FDA 510k Clearance Consulting for Medical Devices and IVD's		</title>
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		<pubDate>Tue, 28 May 2013 09:24:21 +0000</pubDate>
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		<pubDate>Wed, 22 May 2013 09:24:58 +0000</pubDate>
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		Comment on FDA Class I, Class II, Class III Medical Devices by Traditional FDA 510k for Medical Devices and IVD's		</title>
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		Comment on FDA Class I, Class II, Class III Medical Devices by FDA 510(k) Premarket Notification Process		</title>
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		Comment on FDA Medical Device Regulations by FDA 510k Clearance Consulting for Medical Devices and IVD's		</title>
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		Comment on FDA 510(k) Process by How to Determine Substantial Equivalence for an FDA 510k		</title>
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		Comment on FDA 510(k) Process by FDA 510(k) Premarket Notification Process		</title>
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		<dc:creator><![CDATA[FDA 510(k) Premarket Notification Process]]></dc:creator>
		<pubDate>Wed, 22 May 2013 09:03:44 +0000</pubDate>
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