UL Was FDA's Top Third-Party 510(k) Premarketing Submission Reviewer for the Fourth Year in a Row (Market Wire via Yahoo! Finance)
Underwriters Laboratories Inc., a world leader in product safety testing and certification, announced today that UL's Medical Devices Business Unit conducted more 510(k) reviews in 2006 than any other Accredited Person on behalf of the U.S.

PR Newswire Summary of Technology Copy, Feb. 21, 2007 (SYS-CON Media)
Following is a summary of high technology news releases transmitted today by PR Newswire. The full text of these releases is available at the PR Newswire for Journalists, http://media.prnewswire.com/.

Sparta Systems Announces Software for Electronic Submission of Medical Device Reports to Food and Drug Administration ... (SYS-CON Media)
Sparta Systems, Inc. (Sparta), the maker of TrackWise(R), and the market leader in enterprise quality and compliance process management software, today announced that it has released the Beta version of the TrackWise eMDR Submission Manager(TM) software. The add-on software enables medical device companies to electronically submit Medical Device Reports (MDRs) to Food and Drug Administration ...