Underwriters Laboratories, Inc. Was FDA’s Top Third-Party 510(k) Premarketing Submission Reviewer For The Fourth Year In A Row

NORTHBROOK, IL -- (MARKET WIRE) -- February 20, 2007 -- Underwriters Laboratories Inc. (UL), 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. Food & Drug Administration (FDA).