Tempus Receives U.S. FDA 510(k) Clearance For The xR IVD In Vitro Diagnostic Device

-4.40% Pre

Tempus AI

TEM

70.61

71.29

-4.40%

+0.96% Pre

Tempus Receives U.S. FDA 510(k) Clearance For The xR IVD In Vitro Diagnostic Device

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