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Follow-up Letter to the FDA Regarding Use of Experimental Pulse Oximeter Devices in the SUPPORT Study

View as PDF.

Public Citizen presses the Food and Drug Administration for answers to key questions regarding the use of experimental oxygen monitoring devices in the SUPPORT study, which involved extremely premature babies, and the inclusion of one particularly misleading statement in many of the institutional review board-approved SUPPORT study consent forms regarding these devices.

April 7, 2015, View the FDA’s Response.