Device Approval

Known as: Device Approvals, Process, Device Approval, Approval Processes, Device 
Process that is gone through in order for a device to receive approval by a government regulatory agency. This includes any required preclinical or… (More)
National Institutes of Health

Papers overview

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2016
2016
PURPOSE Develop a computer-aided detection (CAD) system for masses in digital breast tomosynthesis (DBT) volume using a deep… (More)
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2015
2015
We propose a novel approach for the detection of microcalcification clusters (MCs) using joint information from digital breast… (More)
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2014
2014
BACKGROUND Medical devices can be useful in a variety of diseases, but few devices have been specifically approved for use in… (More)
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2011
2011
We present a software architecture that federates data from multiple heterogeneous health informatics data sources owned by… (More)
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2010
2010
PURPOSE In digital breast tomosynthesis (DBT), quasi-three-dimensional (3D) structural information is reconstructed from a small… (More)
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2010
2010
The quality of clinical data submitted by manufacturers to support Food and Drug Administration cardiovascular device premarket… (More)
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2009
2009
The purpose of this study was to assess ulnar translation in perilunate dislocation injuries. Twenty-five patients with… (More)
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2008
2008
This article discusses options and examples of regulations or "generally recognized as safe" determinations that are related to… (More)
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Highly Cited
2008
Highly Cited
2008
BACKGROUND Text-based patient medical records are a vital resource in medical research. In order to preserve patient… (More)
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Highly Cited
2004
Highly Cited
2004
Typical high throughput microarrays experiments compare gene expression across two specimen classes – an experimental class and… (More)
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