Hematology and Pathology Devices Panel

Description

The Hematology and Pathology Devices Panel reviews and evaluates data concerning the safety and effectiveness of marketed and investigational in vitro devices for use in clinical laboratory medicine including pathology, hematology, histopathology, cytotechnology and molecular biology and makes appropriate recommendations to the Commissioner of Food and Drugs.

Designated Federal Official (DFO)

Sara J. Anderson
301-796-7047