Original paper

Food and Drug Administration (FDA) Medical Device Reports From 1991 to 2015: Are Radiation Oncology Devices Different?

Volume: 96, Issue: 2, Pages: E394 - E394
Published: Oct 1, 2016
Abstract
The field of radiation oncology relies heavily on rapidly evolving technology and highly complex processes. The FDA collects and records all reported adverse events from medical devices. We sought to characterize all events involving radiation oncology devices (RODs) from the FDA's post-market surveillance MAUDE (Manufacturer and User Facility Device Experience) database, and compare these to other non-radiation oncology devices. MAUDE data was...
Paper Details
Title
Food and Drug Administration (FDA) Medical Device Reports From 1991 to 2015: Are Radiation Oncology Devices Different?
Published Date
Oct 1, 2016
Volume
96
Issue
2
Pages
E394 - E394
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