Stuart Goldman

From This Author

Compliance

Medical Device Testing Requirements for 510(k) Submissions

Clients who engage us for FDA 510(k) submission consulting often ask what testing is required by the FDA to clear their device. While testing requirements are easy to determine for some devices, other devices require intensive research.

Digital Sponsors

Become a Sponsor

What's New

FCC to Vote on Restoring Net Neutrality

Tektronix Expands Catalog of High-Power Test and Measurement Devices

Nominations Open for the EMC Society Board of Directors

How AI is Changing the Regulation of Medical Devices

Averna Acquires Automated Test Solutions Provider ELCOM

- From Our Sponsors -