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Results: 1-6 of 6

FDA accepts 23andMe 510(k) application for single-condition health report
  • Shook Hardy & Bacon LLP
  • USA
  • June 26 2014

The U.S. Food and Drug Administration (FDA) has reportedly accepted for review 23andMe's submission for the premarket approval of a new medical


23andMe founder seeks to empower consumers
  • Shook Hardy & Bacon LLP
  • USA
  • March 20 2014

Speaking during the recently concluded SXSW festival in Austin, Texas, 23andMe co-founder Anne Wojcicki reportedly acknowledged that the U.S. Food


Consumer-fraud class action filed against 23andme after FDA action
  • Shook Hardy & Bacon LLP
  • USA
  • December 12 2013

Citing the Food and Drug Administration's (FDA's) November 22, 2013, warning letter, a California resident has filed a putative class action against


FDA orders 23andme to stop selling DNA tests
  • Shook Hardy & Bacon LLP
  • USA
  • December 12 2013

The U.S. Food and Drug Administration (FDA) issued a warning letter in late November 2013 to 23andMe, Inc., the company that marketed a home "Saliva



Chris A. Johnson
  • Shook Hardy & Bacon LLP