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

    MSI 9000 SERIES BED

    K Number: K873291 · Decision Dec 30, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    228
    Registration Numbers
    228
    Same Product Code
    69
    Applicant Total
    9
    Review Days
    135

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    Basic Information

    Device Name
    MSI 9000 SERIES BED
    K Number
    K873291
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5100
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Med Service, Inc.
    Date Received
    August 17, 1987
    Decision Date
    December 30, 1987
    Product Code
    FNL
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    FNL Bed, Ac-Powered Adjustable Hospital

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    Other Clearances by Med Service, Inc.

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    K881782 MSI 4000 SERIES BED
    K881963 MSI 3002 SERIES BED
    K881964 MSI 3003 SERIES BED
    K881962 MSI 2005 SERIES BED
    K881965 MSI 5000 SERIES BED
    K881027 MSI 2002 SERIES BED