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Automated Pap Screening Gains Recommendation

FDA panel evaluated NeoPath’s AutoPap® System for potential use in primary screening

CEO SUMMARY: Automated cytology technology received a big boost when the FDA’s advisory panel voted to recommend that the FDA approve, with conditions, NeoPath’s AutoPap® System as a primary Pap Smear Screener. The company still awaits final FDA approval on this matter. ON JANUARY 28, the Food And Drug Administration’s (FDA) Hematology and Pathology Devices …

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