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NEW YORK (360Dx) – Sydney, Australia-based SpeeDx said this week that the US Food and Drug Administration has granted Breakthrough Device designation for its ResistancePlus GC molecular test, which could expedite its path toward regulatory clearance. ResistancePlus GC provides ciprofloxacin susceptibility and resistance information to effectively guide treatment for N. gonorrhea, the firm said. The test detects both N.

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