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510(k) Data Aggregation

    K Number
    K250153
    Device Name
    Neu Platform
    Manufacturer
    Neuhealth Digital Ltd.
    Date Cleared
    2025-04-25

    (94 days)

    Product Code
    GYD
    Regulation Number
    882.1950
    Why did this record match?
    Applicant Name (Manufacturer) :

    Neuhealth Digital Ltd.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
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