FDA OKs new UltraSPECT feature

AuntMinnie.com staff writers
Jun 7, 2009

Nuclear medicine firm UltraSPECT of Merrick, NY, has added a U.S. Food and Drug Administration (FDA)-cleared half-dose imaging feature to its Xpress.Cardiac half-time wide-beam reconstruction (WBR) image reconstruction product.

The new feature is designed to minimize radiation exposure to patients, while maximizing safety for patients and medical staff. With the addition, Xpress.Cardiac provides dose and acquisition time management, so rest/stress studies can be acquired using either half the radiopharmaceutical dose or half the scan time.

Related Reading

UltraSPECT nets FDA OK for software, June 2, 2009

UltraSPECT launches new SPECT package, May 1, 2009

Cardinal to sell UltraSPECT packages, April 2, 2008

UltraSPECT reaches U.S. milestone, August 1, 2007

UltraSPECT makes management changes, May 30, 2007

Copyright © 2009 AuntMinnie.com

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