Denise Leung Klinker is a Staff Engineer in the Life and Health Sciences Business unit in UL’s Fremont Office. Leveraging 30 years of experience in the medical device industry, she has assisted clients with a wide range of conformity assessment services, including product safety evaluation, testing, and certifications for a wide variety of medical electrical equipment, laboratory equipment, personal hygiene and health care equipment. Klinker was also a FDA qualified 3rd party 510(K) reviewer and program reviewer. In addition, she serves as an UL instructor for UL public and private seminars on IEC 60601-1, editions 2, 3, and 3.1. She holds a BS in Electrical Engineering from University of the Pacific.