Try our Advanced Search for more refined results

Medical Device Makers Urge FDA To Narrow ID Rule

By Rachel Slajda (November 8, 2012, 5:07 PM EST) -- The medical device industry on Wednesday urged the Food and Drug Administration to scale back its proposed unique device identification rule aimed at tracking devices and improving recalls, arguing that plans to require the direct marking of implantable devices is illogical and impractical....

Law360 is on it, so you are, too.

A Law360 subscription puts you at the center of fast-moving legal issues, trends and developments so you can act with speed and confidence. Over 200 articles are published daily across more than 60 topics, industries, practice areas and jurisdictions.


A Law360 subscription includes features such as

  • Daily newsletters
  • Expert analysis
  • Mobile app
  • Advanced search
  • Judge information
  • Real-time alerts
  • 450K+ searchable archived articles

And more!

Experience Law360 today with a free 7-day trial.

Start Free Trial

Already a subscriber? Click here to login

Attached Documents

Related Sections

Companies

Government Agencies

Hello! I'm Law360's automated support bot.

How can I help you today?

For example, you can type:
  • I forgot my password
  • I took a free trial but didn't get a verification email
  • How do I sign up for a newsletter?
Ask a question!