CardiArc seeks clearance for SPECT

AuntMinnie.com staff writers
Nov 22, 2005

Cardiac imaging device developer CardiArc reported that it submitted a premarket notification 510(k) application with the Food and Drug Administration for a SPECT imaging device last month.

The Lubbock, TX-based CardiArc said the SPECT device has been specifically designed for use in outpatient settings. In its present configuration, the device fits within a 6 x 7-foot exam room, requires no room modifications for installation or operation, and uses U.S. standard voltage.

By AuntMinnie.com staff writers
November 23, 2005

Related Reading

CardiArc signs investment banker, September 5, 2005

Copyright © 2005 AuntMinnie.com

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