Medical Devices & the FDA - Regulation, User Fees & Tort Claims (Paperback)

Medical device regulation is complex, in part because of the wide variety of items that are categorized as medical devices. They may be simple tools used during medical examinations, such as tongue depressors and thermometers, or high-tech life-saving implants like heart valves and coronary stents. The medical device market has been characterized as including eight industry sectors: surgical and medical instrument manufacturing, surgical appliance and supplies, in vitro diagnostic products (IVDs, or laboratory tests), electromedical and electrotherapeutic apparatus, irradiation apparatus, dental equipment and supplies, ophthalmic goods, and dental laboratories. This book explores FDA regulation of medical devices with a focus on the user fee program and tort claims.

General

Imprint:	nova science publishers
Country of origin:	United States
Release date:	March 2013
First published:	March 2013
Editors:	Gil Frazier • Brady Malone
Dimensions:	230 x 155 x 8mm (L x W x T)
Format:	Paperback
Pages:	127
ISBN-13:	978-1-62257-674-6
Categories:	Books > Medicine > Nursing & ancillary services > Biomedical engineering > General
LSN:	1-62257-674-8
Barcode:	9781622576746

Is the information for this product incomplete, wrong or inappropriate? Let us know about it.

Does this product have an incorrect or missing image? Send us a new image.

Is this product missing categories? Add more categories.

Review This Product

No reviews yet - be the first to create one!