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10.1186/s12906-022-03645-7 51 HouJ.ZhengD.ZhongG.HuY
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Electrochemical sensors: core principle, new fabrication trends, and their applications, in Biosensors in food safety and quality
doi: 10.1080/14756366.2024.2301768
The 510(k) clearance process refers to a premarket submission made to the FDA to demonstrate that a new medical device is substantially equivalent to a legally marketed predicate device [129]
