Proposed Guidelines for Primary Instruments for Gynecologic Cytology
The FDA Pathology Devices Advisory Panel unanimously recommended that the FDA approve with conditions the supplement to the pre-market approval (PMA) submission to use the AutoPap System as a PRIMARY Pap Smear Screener.
International Academy of Cytology updates device guidelines for designers of automated systems.
Authors' Financial Disclosures Required for Manuscripts Submitted After December 31, 1997
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