The US FDA 510(k) database is a centralized repository of all US FDA 510(k) submissions, clearances, and approvals. Hence, medical device manufacturers are required to refer to the US FDA 510(k) database preparing for FDA 510(k) clearance. Information from the...
The US FDA 510(k) approval process authorizes the marketing of IVDs in the US. Through this process the Food and Drug Administration (FDA) evaluates device safety and effectiveness before releasing it in the market. Hence, compliance with US FDA...
Planning to market your medical device in the US? Then, you will have to secure the US FDA 510(k) approval. For which you will require proper documentation and have to select the appropriate predicate device. You will need the predicate device to prove substantial...