The Anesthesiology and Respiratory Therapy Devices Panel (ARTDP)reviews and evaluates data concerning the safety and effectiveness of marketed and investigational devices for use in anesthesiology and respiratory therapy and makes appropriate recommendations to the Commissioner of Food and Drugs.
Designated Federal Officer (DFO)
Candace Nalls, M.P.H.
- FDA Advisory Committee Information Line
- (301-443-0572 in the Washington DC area)
Please call the Information Line for up-to-date information on this meeting.