Adverse Events Involving Radiation Oncology Medical Devices: Comprehensive Analysis of US Food and Drug Administration Data, 1991 to 2015.

Abstract

PURPOSE Radiation oncology relies on rapidly evolving technology and highly complex processes. The US Food and Drug Administration collects reports of adverse events related to medical devices. We sought to characterize all events involving radiation oncology devices (RODs) from the US Food and Drug Administration's postmarket surveillance Manufacturer and… (More)
DOI: 10.1016/j.ijrobp.2016.08.050

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Cite this paper

@article{Connor2017AdverseEI, title={Adverse Events Involving Radiation Oncology Medical Devices: Comprehensive Analysis of US Food and Drug Administration Data, 1991 to 2015.}, author={Michael Connor and Deborah C. Marshall and Vitali Moiseenko and Kevin Moore and Laura Cervino and Todd C. Atwood and Parag R Sanghvi and Arno J. Mundt and Todd Pawlicki and Abram Recht and Jona A. Hattangadi-Gluth}, journal={International journal of radiation oncology, biology, physics}, year={2017}, volume={97 1}, pages={18-26} }