DocumentCode
744759
Title
What´s in a 510(k)? [medical device marketing]
Author
Munzner, Robert
Volume
22
Issue
3
fYear
2003
Firstpage
157
Lastpage
158
Abstract
If you hope to market a new medical device in the United States, sending a premarket notification, or 510(k) is probably the easiest and fastest way to do so. The article briefly looks at the 510(k) and outlines what it is, gives guidelines for preparing it including useful resources, and gives an idea of fees and review time required.
Keywords
biomedical equipment; legislation; 510(k); FDA; United States; legal requirements; medical device; premarket notification; regulatory issues;
fLanguage
English
Journal_Title
Engineering in Medicine and Biology Magazine, IEEE
Publisher
ieee
ISSN
0739-5175
Type
jour
DOI
10.1109/MEMB.2003.1213643
Filename
1213643
Link To Document