Cybersecurity features of digital medical devices: an analysis of FDA product summaries

OBJECTIVES: To more clearly define the landscape of digital medical devices subject to US Food and Drug Administration (FDA) oversight, this analysis leverages publicly available regulatory documents to characterise the prevalence and trends of software and cybersecurity features in regulated medica...

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Detalles Bibliográficos
Autores principales: Stern, Ariel Dora, Gordon, William J, Landman, Adam B, Kramer, Daniel B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Health Informatics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609083/
https://www.ncbi.nlm.nih.gov/pubmed/31256020
http://dx.doi.org/10.1136/bmjopen-2018-025374

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609083/
https://www.ncbi.nlm.nih.gov/pubmed/31256020
http://dx.doi.org/10.1136/bmjopen-2018-025374

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