This paper is in the following e-collection/theme issue:

Regulatory Issues and Medical Device Certification (4) Policy and Policy Proposals (133) Safety and Error Prevention in Health (214) Development of Novel Medical Devices and Innovations for Existing Devices (84) Medical Device Adverse Events, Errors, Safety (17)

Published on in Vol 6, No 4 (2021): Oct-Dec

Preprints (earlier versions) of this paper are available at https://preprints.jmir.org/preprint/20652, first published .
Tracking the Presence of Software as a Medical Device in US Food and Drug Administration Databases: Retrospective Data Analysis

Tracking the Presence of Software as a Medical Device in US Food and Drug Administration Databases: Retrospective Data Analysis

Tracking the Presence of Software as a Medical Device in US Food and Drug Administration Databases: Retrospective Data Analysis

Authors of this article:

Aaron Ceross1 Author Orcid Image ;   Jeroen Bergmann1 Author Orcid Image
Article Authors Cited by (2) Tweetations (2) Metrics

Journals

  1. Freyer O, Wrona K, de Snoeck Q, Hofmann M, Melvin T, Stratton-Powell A, Wicks P, Parks A, Gilbert S. The regulatory status of health apps that employ gamification. Scientific Reports 2024;14(1) View

Books/Policy Documents

  1. Uddin M, Ge M. Information and Communication Technologies for Ageing Well and e-Health. View