BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    Digital Routines

    K Number: K221924 · Decision Mar 15, 2023
    View on FDA
    Classifications
    1
    FEI Numbers
    34
    Registration Numbers
    34
    Same Product Code
    54
    Applicant Total
    1
    Review Days
    257

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    Basic Information

    Device Name
    Digital Routines
    K Number
    K221924
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.1890
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Gnc Holdings, LLC
    Date Received
    July 1, 2022
    Decision Date
    March 15, 2023
    Product Code
    NDC
    Advisory Committee
    Anesthesiology
    Review Advisory Committee
    CH
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    NDC Calculator, Drug Dose

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