Identification and Market Removal of Risky Medical Devices-Reference-Cited by-同舟云学术

Identification and Market Removal of Risky Medical Devices

Published:2020-11-01 Issue:11 Volume:180 Page:1426
ISSN:2168-6106
Container-title:JAMA Internal Medicine
language:en
Short-container-title:JAMA Intern Med

Author:

Tomes Madris¹

Affiliation:

1. Device Events, York, Pennsylvania

Publisher

American Medical Association (AMA)

Subject

Internal Medicine

Link

https://jamanetwork.com/journals/jamainternalmedicine/articlepdf/2771088/jamainternal_tomes_2020_ic_200023_1603479543.15402.pdf

Reference3 articles.

1. Assessment of data sources that support US Food and Drug Administration medical devices safety communications.;Tau;JAMA Intern Med

2. Miscategorization of deaths in the US Food and Drug Administration adverse events database.;Meier;JAMA Intern Med,2019

3. Medical Device Guardian Act, HR 2915, 116th Cong (2020). Accessed August 6, 2020. https://www.congress.gov/bill/116th-congress/house-bill/2915/text?r=39&s=1

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