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

    DIGITAL BABY SCALE MODEL BLB-12

    K Number: K932572 · Decision Nov 16, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    98
    Registration Numbers
    98
    Same Product Code
    47
    Applicant Total
    6
    Review Days
    173

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    Basic Information

    Device Name
    DIGITAL BABY SCALE MODEL BLB-12
    K Number
    K932572
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.2720
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Tanita Corp. of America
    Date Received
    May 27, 1993
    Decision Date
    November 16, 1993
    Product Code
    FRW
    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
    FRW Scale, Patient

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