Digirad gets FDA nod for nSpeed

AuntMinnie.com staff writers
Sep 22, 2008

Nuclear medicine vendor Digirad has received U.S. Food and Drug Administration (FDA) 510(k) clearance for its nSpeed reconstruction software.

nSpeed is designed to improve image quality and reduce imaging time for SPECT procedures, according to the Poway, CA-based firm.

Related Reading

Trial begins for Digirad's Cardius X-ACT, September 5, 2008

Novel cardiac SPECT system improves attenuation correction, August 15, 2008

Digirad posts loss in Q2, July 29, 2008

Digirad signs deal with U. of Chicago, April 29, 2008

Digirad Q1 results dip into red, April 24, 2008

Copyright © 2008 AuntMinnie.com

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