"Device Approval" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Process that is gone through in order for a device to receive approval by a government regulatory agency. This includes any required preclinical or clinical testing, review, submission, and evaluation of the applications and test results, and post-marketing surveillance. It is not restricted to FDA.
| Descriptor ID |
D018795
|
| MeSH Number(s) |
E05.337.275 N06.850.210.275
|
| Concept/Terms |
Device Approval- Device Approval
- Approval, Device
- Approvals, Device
- Device Approvals
- Device Approval Process
- Approval Process, Device
- Approval Processes, Device
- Device Approval Processes
- Process, Device Approval
- Processes, Device Approval
New Device Approval- New Device Approval
- Approval, New Device
- Approvals, New Device
- Device Approval, New
- Device Approvals, New
- New Device Approvals
|
Below are MeSH descriptors whose meaning is more general than "Device Approval".
Below are MeSH descriptors whose meaning is more specific than "Device Approval".
This graph shows the total number of publications written about "Device Approval" by people in this website by year, and whether "Device Approval" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2006 | 0 | 1 | 1 |
| 2012 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2015 | 0 | 1 | 1 |
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Below are the most recent publications written about "Device Approval" by people in Profiles.
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Lum F, Tarver ME, Kahook MY, Oetting TA, Rorer E, Hilmantel G, Calogero D, Kiang T, Berdahl JP, Coleman AL, Eydelman MB. Special Commentary: Food and Drug Administration and American Academy of Ophthalmology Sponsored: Developing Novel End Points for Premium Intraocular Lenses Workshop. Ophthalmology. 2015 Jul; 122(7):1522-31.
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Zinn AM, Allen JC, Hacker CS. New medical devices: the author's reply to Brock. Health Aff (Millwood). 2013 Jan; 32(1):192-3.
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Zinn AM, Allen JC, Hacker CS. Median approval times for class III medical devices have been well above statutory deadlines set for FDA and CMS. Health Aff (Millwood). 2012 Oct; 31(10):2304-13.
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Krummel TM, Gertner M, Makower J, Milroy C, Gurtner G, Woo R, Riskin DJ, Binyamin G, Connor JA, Mery CM, Shafi BM, Yock PG. Inventing our future: training the next generation of surgeon innovators. Semin Pediatr Surg. 2006 Nov; 15(4):309-18.