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# CDRH Industry Basics Webcast
- URL: https://www.fdaweb.com/cdrh-industry-basics-webcast/
- Published: 2019-12-04T12:00:00.000Z
- Updated: 2026-09-14T15:55:23.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5145650

A recent CDRH Industry Basics Webcast covered Webpage and multimedia resources available for industry on a variety of CDRH topics and then gave basic information on the 513(g) request for information process and the custom device exemption process.

In the [show’s](http://fda.yorkcast.com/webcast/Play/626be66734eb406f986cdda0005a306a1d?ref=fdaweb.com) first hour, CDRHer **Ifearyi Uwemedimo** discussed how the 513(g) process is used when industry is unsure of a device determination and classification. In the second hour, CDRHer **Nathan Ivey** introduced the custom device exemption program and its reporting requirements. Each segment also included a panel of Center experts who responded to viewers’ questions when the show aired.