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

    WH ACCU TEST ONE-STEP URINE/SERUM COMBO PREGNANCY TEST

    K Number: K051841 · Decision Aug 22, 2005
    View on FDA
    Classifications
    1
    FEI Numbers
    102
    Registration Numbers
    102
    Same Product Code
    374
    Applicant Total
    14
    Review Days
    46

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    Basic Information

    Device Name
    WH ACCU TEST ONE-STEP URINE/SERUM COMBO PREGNANCY TEST
    K Number
    K051841
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1155
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    W.H.P.M., Inc.
    Date Received
    July 7, 2005
    Decision Date
    August 22, 2005
    Product Code
    JHI
    Advisory Committee
    Clinical Chemistry
    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
    JHI Visual, Pregnancy Hcg, Prescription Use

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