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Neopath files initial screening premarket approval application (PMA) for AutoPap

This article was originally published in Clinica

Executive Summary

Neopath (US) has filed a new PMA with the US FDA to allow its AutoPap slide reader to be used for initial cervical screening. The FDA's haematology and pathology devices panel will review the application - for initial screening of all Pap smear slides processed by a clinical laboratory - on September 27th.

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