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

    TARGET(TM) HOG ONE STEP

    K Number: K903937 · Decision Oct 22, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    102
    Registration Numbers
    102
    Same Product Code
    374
    Applicant Total
    22
    Review Days
    56

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    Basic Information

    Device Name
    TARGET(TM) HOG ONE STEP
    K Number
    K903937
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1155
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    V-Tech, Inc.
    Date Received
    August 27, 1990
    Decision Date
    October 22, 1990
    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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    Other Clearances by V-Tech, Inc.

    K Number Device Name
    K914303 TARGET(TM)-HOG
    K910893 TARGET(TM) CANNABINOIDS-R TEST
    K910892 TARGET(TM) CANNABINOIDS-V TEST
    K910739 TARGET AMPHETAMINE/METHAMPHETAMINE-R (READER METH)
    K910738 TARGET AMPHETAMINE/METHAMPHETAMINE-V (VISUAL METH)
    K910122 TARGET COCAINE METABOLITE-R
    K910123 TARGET COCAINE METABOLITE-V
    K890978 TARGET OPIATES-R
    K890979 TARGET OPIATES-V
    K890295 TARGET(TM) CK-MB
    Search all 22 clearances from V-Tech, Inc. →