We will explain what a 510(k) is and the procedure to prepare the submission. The several types of 510(k) will be explained. Each part of the submission will be explained. The very confusing concepts of predicate device and substantial equivalence will be discussed. How to find an acceptable predicate device will be taught. FDA places special emphasis on-device software. we will cover the requirements for software.
Areas Covered
Who Should Attend
Why Should You Attend
Preparing a submission to get FDA approval for a new product is time-consuming and confusing. The submission requirements refer to many unfamiliar concepts and terms. More than half of all submissions are rejected. We will teach you to prepare a submission meets all the FDA requirements.
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