United States, May 5 -- GE HealthCare is proud to announce that the U.S. Food and Drug Administration (FDA) granted 510(k) clearance of its impressive Aurora nuclear medicine system and Clarify DL. This advanced dual-head SPECT/CT is designed to enhance diagnostic capabilities[i] and streamline workflows, offering clinicians excellent image quality and operational efficiency.As healthcare continues to shift toward precision medicine and personalized care, clinicians require more advanced SPECT/CT solutions that provide greater diagnostic accuracy and efficiency. The ability to monitor and help tailor treatments to individual patients depends on high-quality imaging that can detect subtle disease markers with confidence. To meet these evolvi...