Reporting Device-Associated Death Events to the FDA-Reply
JAMA Intern Med
.
2022 Apr 1;182(4):462-463.
doi: 10.1001/jamainternmed.2021.8512.
Authors
Christina Lalani
1
,
Madris Kinard
2
,
Rita F Redberg
3
4
Affiliations
1
Department of Medicine, University of California, San Francisco.
2
Device Events LLC, York, Pennsylvania.
3
Department of Medicine, Division of Cardiology, University of California, San Francisco.
4
Editor, JAMA Internal Medicine.
PMID:
35188530
DOI:
10.1001/jamainternmed.2021.8512
No abstract available
Publication types
Comment
MeSH terms
Databases, Factual
Device Approval*
Equipment Safety
Humans
Product Surveillance, Postmarketing*
United States
United States Food and Drug Administration