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      • And more…
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      • Performance evaluation of IVDs
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      • FDA relevant documents
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October 24, 2023


Predicate device & substantial equivalence

By Luca SalvatoreOctober 24, 2023Leave a comment

The term “predicate device” most often comes up in the context of FDA 510(k) clearances. However, the FDA does not define this term. It does, however, define what “substantial equivalence” is. Sounds complicated? Demonstrating equivalence is by no means only relevant in the FDA context. That’s why this article provides clarity – especially but not…

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FDA: The 510(k) clearance (Premarket Notification)

By Luca SalvatoreOctober 24, 2023Leave a comment

510(k) clearance is the primary procedure for obtaining marketing clearance in the United States. It is also referred to as Premarket Notification (PMN). This article provides a quick overview of the procedure and the documents that must be submitted.

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