510(k) Clinical Data Insights: What It Means for FDA 510(k) Submissions Explore how clinical data fits into FDA 510(k) submissions and its role in demonstrating substantial equivalence to a predicate device. While most 510(k)s rely on non-clinical performance data, clinical data may be required when safety or effectiveness questions can’t be fully addressed by bench or animal testing. This guide breaks down when clinical evidence is needed, what types of data might be included, and how it supports the FDA’s review process for medical device clearance. Learn key considerations for organizing and presenting clinical results alongside other required information in your 510(k) submission. Visit us: https://www.bioaccessla.com/blog/understanding-fda-approval-a-guide-to-510-k-submissions