The New 510(k) Paradigm Alternate Approaches to Demonstrating Substantial Equivalence in Premarket Notifications

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Health Investigational Device Exemption Premarket approval Medical device Federal Food Drug and Cosmetic Act Food and Drug Administration Modernization Act Center for Devices and Radiological Health Design controls Validation Food and Drug Administration Medicine Technology		The New 510(k) Paradigm Alternate Approaches to Demonstrating Substantial Equivalence in Premarket Notifications Add to Reading List Source URL: www.fda.gov Download Document from Source Website File Size: 57,86 KB Share Document on Facebook

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