BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇲🇾 Malaysia

    PATIENT LATEX EXAMINATION POWDER-FREE POLYMER COATED GLOVES

    K Number: K992676 · Decision Dec 16, 1999
    View on FDA
    Classifications
    1
    FEI Numbers
    151
    Registration Numbers
    151
    Same Product Code
    1953
    Applicant Total
    8
    Review Days
    128

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    Basic Information

    Device Name
    PATIENT LATEX EXAMINATION POWDER-FREE POLYMER COATED GLOVES
    K Number
    K992676
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.6250
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Wear Safe Malaysia Sdn. Bhd.
    Date Received
    August 10, 1999
    Decision Date
    December 16, 1999
    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 Wear Safe Malaysia Sdn. Bhd.

    K Number Device Name
    K062917 STERILE AND NON-STERILE POWDER-FREE LATEX PATIENT EXAMINATION GLOVE, WITH EXTRACTABLE PROTEIN CONTENT LABELING CLAIM (50
    K062778 STERILE POWDER-FREE NITRILE PATIENT EXAMINATION GLOVE, BLUE COLORED
    K992675 PATIENT NITRILE EXAMINATION GLOVES (POWDERED)
    K992681 PATIENT LATEX EXAMINATION GLOVE POWDERED & POWDER FREE, STERILE
    K992678 PATIENT NITRILE EXAMINATION GLOVES POWDER FREE CHLORINATED
    K992679 SURGEON POWDER-FREE GLOVES, LATEX, STERILE
    K973020 PATIENT EXAMINATION POWDER-FREE GLOVES