• 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