Nuclear medicine firm UltraSPECT said it has received clearance from the U.S. Food and Drug Administration (FDA) for its whole-body PET imaging reconstruction application.
Xpress.PET is based on UltraSPECT's wide-beam reconstruction technology, which enables reduced radiopharmaceutical dose and acquisition time, according to UltraSPECT.
The company plans to offer Xpress.PET immediately in the U.S.