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  • FDA Issues Draft Guidance on 510(k) Transfer Protocols for Biotech and MedTech Firms

    In June 2025, the U.S. Food and Drug Administration (FDA) issued a long-anticipated draft guidance that clarifies the process for transferring ownership of 510(k) clearances. The document: “Transfer of a Premarket Notification (510(k)) Clearance” addresses [...]

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