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

    SRI HUMAN CHORIONIC GONADOTROPIN IMMUNOENZ ASSAY

    K Number: K894175 · Decision Dec 19, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    102
    Registration Numbers
    102
    Same Product Code
    374
    Applicant Total
    23
    Review Days
    187

    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
    SRI HUMAN CHORIONIC GONADOTROPIN IMMUNOENZ ASSAY
    K Number
    K894175
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1155
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Serono-Baker Diagnostics, Inc.
    Date Received
    June 15, 1989
    Decision Date
    December 19, 1989
    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 Serono-Baker Diagnostics, Inc.

    K Number Device Name
    K924257 TESTOSTERONE SEROZYME(TM) ENZYME IMMUNOASSAY
    K915164 SRI TESTOSTERONE ENZYME IMMUNOASSAY
    K914886 SRI(TM) CORTISOL ENZYME IMMUNOASSAY(MAG SOL PHASE)
    K915602 SRI DIGOXIN ENZYME IMMUNOASSAY
    K912937 SR1 FREE T4 ENZYME IMMUNOASSAY
    K914462 SRI PROGESTERONE ENZYME IMMUNOASSAY(MAG SOLD PHAS)
    K911912 SR1 T3 UPTAKE ENZYME IMMUNOASSAY(MAG SOLID-PHASE)
    K911217 SR1 T4 ENZYME IMMUNOASSAY (MAGNETIC SOLID-PHASE)
    K912318 ESTRADIOL SEROZYME ENZYME IMMUNO (MAG SOLID-PHASE)
    K911396 SR1 ESTRADIOL ENZYME IMMUNOASSAY
    Search all 23 clearances from Serono-Baker Diagnostics, Inc. →