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The FocalPoint system includes the U.S. Food and Drug Administration (FDA)-approved FocalPoint Slide Profiler, a computerized scanning device that performs analyses of cervicovaginal cytology samples, and the FocalPoint GS, a system that currently is under evaluation by the FDA and that adds location-guided screening capabilities to the FocalPoint Slide Profiler.
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Thomas F. Kardos (2004) studied this question.
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