BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇦 Canada

    AFP MIDDLEBROOK 7H10 AGAR SLANT

    K Number: K872676 · Decision Aug 11, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    24
    Registration Numbers
    24
    Same Product Code
    306
    Applicant Total
    29
    Review Days
    35

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    Basic Information

    Device Name
    AFP MIDDLEBROOK 7H10 AGAR SLANT
    K Number
    K872676
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    866.2360
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    I.A.F. Production, Inc.
    Date Received
    July 7, 1987
    Decision Date
    August 11, 1987
    Product Code
    JSJ
    Advisory Committee
    Microbiology
    Review Advisory Committee
    MI
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    JSJ Culture Media, Selective And Non-Differential

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    Other Clearances by I.A.F. Production, Inc.

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    K872675 IAFP MANNITOL NACL
    K872669 IAFP X.L.D. AGAR
    K872683 IAFP BILE ESCULIN AGAR
    K872672 IAFP BILE ESCULIN AZIDE AGAR
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