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

    POWDERED PATIENT EXAMINATION GLOVES, LATEX

    K Number: K001715 · Decision Jul 5, 2000
    View on FDA
    Classifications
    1
    FEI Numbers
    151
    Registration Numbers
    151
    Same Product Code
    1953
    Applicant Total
    6
    Review Days
    30

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    Basic Information

    Device Name
    POWDERED PATIENT EXAMINATION GLOVES, LATEX
    K Number
    K001715
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.6250
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Fitco Dipped Products Pvt., Ltd.
    Date Received
    June 5, 2000
    Decision Date
    July 5, 2000
    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 Fitco Dipped Products Pvt., Ltd.

    K Number Device Name
    K001232 NON-STERILE POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN LABELING CLAIM 50 MICROGRAMS OR LESS
    K000896 POWDERFREE LATEX SURGEON'S GLOVES WITH PROTIEN LABELING CLAIM (50 MOCROGRAMS OR LESS
    K001216 POWDER-FREE LATEX EXAMINATION GLOVE STERILE WITH OPTIONAL PROTEIN LABELING CLAIM (50 MICROGRAMS OR LESS)
    K000891 STERILE LATEX POWDERED PATIENT EXAMINATION GLOVES
    K993450 LATEX SURGICAL GLOVES, PRE-POWDERED