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 :
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