BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    LATEX EXAMINATION GLOVES (MFG. NINGBO MEDICAL)

    K Number: K890891 · Decision Jul 14, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    151
    Registration Numbers
    151
    Same Product Code
    1953
    Applicant Total
    11
    Review Days
    142

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    Basic Information

    Device Name
    LATEX EXAMINATION GLOVES (MFG. NINGBO MEDICAL)
    K Number
    K890891
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.6250
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Interpro Intl., Inc.
    Date Received
    February 22, 1989
    Decision Date
    July 14, 1989
    Product Code
    LYY
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    LYY Latex Patient Examination Glove

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    Other Clearances by Interpro Intl., Inc.

    K Number Device Name
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    K891438 PATIENT EXAMINATION GLOVES (LATEX)
    K891440 PATIENT EXAMINATION GLOVES (LATEX)
    K881374 SURGEONS GLOVES
    K874067 GUAZE SPONGES
    K874766 INTERPRO INT'L, INC. ISOLATION GOWN
    K874066 SURGICAL CAPS
    K874064 SHOE COVERS
    K874065 LAPAROTOMY SPONGES
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