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Medical Device Safety Action Plan: Protecting Patients, Promoting Public Health.

June 6, 2018

Silver Spring, MD: US Food and Drug Administration; April 2018.

Reliable use of medical devices is an important contributor to safe health care delivery. This report describes the US Food and Drug Administration's Center for Devices and Radiological Health (CDRH) plan to raise awareness of problems with devices in the field, develop new devices with better safety and cybersecurity protections, and enhance innovation and the product life cycle through regulation.

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Facility and Group Administrators

Device-Related Complications

Epidemiology of Errors and Adverse Events

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