Empowering Trust™

Meeting FDA Expectations for ISO 18562 VOC and Particle Testing for Medical Devices

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Learn about US FDA 510(K), a premarket notification program that helps demonstrate the safety and effectiveness of a medical device in support of its intended use in the U.S.

In this webinar recording delivered live on June 6 2017, Scott Steady, a UL expert in the area of Environmental testing, provided an overview of the series of standards, the scope, testing required and best practices.

Presenter

Scott Steady: senior product manager, UL Environment

Scott Steady graduated from Louisiana State University with a bachelor’s degree in chemical engineering. He has worked as an air quality consultant helping industrial facilities comply with the EPA’s Clean Air Act regulations. For the past 15 years, Scott has been working with product manufacturers to help them understand their products impact on chemical exposure and health. He participated in the development of chemical emissions test methods for UL’s GREENGUARD Certification Program, the BIFMA furniture emissions standards and many other product related sustainability initiatives.

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General single column text area spanning width of page with 500-character count sample length. Text may contain bullets, numbered lists, text links. Here is a great place to use our messaging framework. UL applies science and objective authority to help people navigate market risk and complexity, and advance the responsible development, production, marketing, and use of the world’s products and innovations.


  • Enhance sustainability
  • Build workplace excellence
  • Protect brand reputation
  • Advance societal well-being
  • Deliver quality and performance
  • Confirm conformance
  • Demonstrate safety
  • Manage transparency
  • Strengthen security
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