BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    STRYKER DYNAMIC MATTRESS SYSTEM (DMS) MODEL #2500

    K Number: K920526 · Decision Sep 21, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    3
    Registration Numbers
    3
    Same Product Code
    2
    Applicant Total
    14
    Review Days
    230

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    Basic Information

    Device Name
    STRYKER DYNAMIC MATTRESS SYSTEM (DMS) MODEL #2500
    K Number
    K920526
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    890.5370
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Stryker Medical
    Date Received
    February 4, 1992
    Decision Date
    September 21, 1992
    Product Code
    IOG
    Advisory Committee
    Physical Medicine
    Review Advisory Committee
    PM
    Third Party
    N

    Classifications

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

    Product Code Device Name
    IOG Treadmill, Mechanical

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