BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇮🇳 India

    LATEX PATIENT EXAMINATION GLOVES

    K Number: K900811 · Decision Mar 9, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    151
    Registration Numbers
    151
    Same Product Code
    1953
    Applicant Total
    5
    Review Days
    16

    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
    LATEX PATIENT EXAMINATION GLOVES
    K Number
    K900811
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.6250
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Kenwell International , Ltd.
    Date Received
    February 21, 1990
    Decision Date
    March 9, 1990
    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

    Similar 510(k) Clearances

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

    Powder Free Natural Rubber Latex Examination Gloves – Blue, Non-Sterile and Protein Claim Of 50 Micrograms per dm2 Or Less Protein

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Latex Examination Glove Powder Free (Ocean Blue and Natural White)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Powder Free Latex Patient Examination Glove, Black Colored, Non-sterile, with Protein Content labeling Claim (Contains 50 ug per dm2 of glove or less of Total Water Extractable Protein)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Sterile Latex Examination Gloves Powder Free (S, M, L, Extra L)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Powder-Free Latex examination gloves

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Non Sterile Powder Free Latex Examination Glove

    FDA 510(k)
    FDA Class 1 ·General Hospital
    View all

    Other Clearances by Kenwell International , Ltd.

    K Number Device Name
    K980412 COLOURED POWDWR-FREE SURGICAL GLOVES
    K980803 STERILE POWDER-FREE LATEX EXAMINATION GLOVES
    K963020 GLOVEL GX
    K911134 SURGICAL GLOVES