Syntermed, Inc. 333 Sandy Springs Circle NE, Suite 107, Atlanta, GA 30328 | Tel (888) 263-4446 | Fax (888) 216-7511

 

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Syntermed medical devices are in compliance with FDA (Quality System Records/Pre-Market Notfication 510(k)) and European Union (ISO 13485:2016 FM 670241/CE Mark 696491) regulations.  See IFU for ECTb and NeuroQ.

 

 

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Syntermed's NeuroQ™ 3.7 for SPECT Brain Imaging to Be Previewed at SNMMI

May 31, 2014

In 2013 Syntermed, Inc. received 510K clearance from the Food and Drug Administration for NeuroQ™ 3.6, software used in nuclear medicine clinics for PET-FDG brain scans plus an additional clearance for the its amyloid brain uptake imaging application. As a work in progress, that 510K clearance extends to Syntermed’s newest nuclear medicine software, NeuroQ 3.7 for SPECT brain imaging quantification.

 

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