Missing information and deficiencies in your 510(k) submission can lead to failure and may significantly delay your medical device product launch. This course is designed to provide an overview of the FDA’s medical device regulations and teach you how to prepare your 510(k).

Join us June 11th, 2025 from 1pm - 4pm Eastern.

The cost for the training is $499 USD. Please complete the form below and we will follow-up with you after registration where you can pay via credit card or purchase order.