REMINDER: Feedback and Comments on 510(k) Preliminary Reports Due By October 4

Several weeks ago, we issued a blog post and an industry alert advising members of the medical device industry of the opportunity to participate in an informational podcast being held by CDRH.  In that post, we also advised you that the preliminary reports on changes to the 510(k) process had been opened for comment by FDA.  FDA relies heavily on industry discussion and comment before finalizing its procedures and reports, but it can't do that if you as an industry participant do not stand up and make your voice heard.

FDA will be accepting comments on "Center for Devices and Radiological Health Preliminary Internal Evaluations" until October 4, 2010, which is only a few short weeks away.  You can submit your comments by writing to the Division of Dockets Management (HFA-305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852, or online through

Trackbacks (0) Links to blogs that reference this article Trackback URL
Comments (0) Read through and enter the discussion with the form at the end
Post A Comment / Question Use this form to add a comment to this entry.

Remember personal info?
Send To A Friend Use this form to send this entry to a friend via email.