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

    PROCLINIC ONE STEP PREGNANCY TEST

    K Number: K914253 · Decision Oct 11, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    102
    Registration Numbers
    102
    Same Product Code
    374
    Applicant Total
    10
    Review Days
    18

    Research this 510(k) in seconds

    The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Device Name
    PROCLINIC ONE STEP PREGNANCY TEST
    K Number
    K914253
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1155
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Vanguard Biomedical Corp.
    Date Received
    September 23, 1991
    Decision Date
    October 11, 1991
    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

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (JHI), ordered by most recent decision date.

    Innovita HCG Pregnancy Rapid Combo Test

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Alltest Pregnancy Rapid Combo Test Cassette

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Atellica IM Total hCG (ThCG)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    TrueDX hCG Early Result Pregnancy Test (Midstream Format), TrueDX hCG Early Result Pregnancy Test (Cassette Format), VeriClear Early Result Pregnancy Test (Midstream Format), VeriClear Early Result Pregnancy Test (Cassette Format)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Assure Tech hCG Pregnancy Serum/Urine Combo Test Cassette, Assure Tech hCG Pregnancy Serum/Urine Combo Test Strip

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    WUNDER PREGNANCY TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry
    View all

    Other Clearances by Vanguard Biomedical Corp.

    K Number Device Name
    K960733 MINISTICK PREGNANCY TEST
    K960233 MINICLINIC OVULATION PREDICTOR
    K930014 PROCLINIC ONE-STEP DIPSTICK PREGNANCY TEST
    K914254 HOMECLINIC ONE STEP PREGNANCY TEST
    K910351 MINICLINIC OVULATION PREDICTION TEST
    K895560 MODIFIED HOMECLINIC PREGNANCY TEST
    K894012 MINICLINIC PREGNANCY TEST
    K891762 MINICLINIC OVULATION PREDICTION TEST
    K883826 HOME CLINIC PREGNANCY TEST