BEUDAMED
    FDA 510(k) FDA unclassified Substantially Equivalent for Some Indications 🇨🇦 Canada

    DUMEX WET DRESSINGS

    K Number: K950132 · Decision Mar 1, 1995
    View on FDA
    Classifications
    1
    FEI Numbers
    384
    Registration Numbers
    385
    Same Product Code
    702
    Applicant Total
    13
    Review Days
    47

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    Basic Information

    Device Name
    DUMEX WET DRESSINGS
    K Number
    K950132
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent for Some Indications
    Applicant
    Dumex Medical Surgical Products, Ltd.
    Date Received
    January 13, 1995
    Decision Date
    March 1, 1995
    Product Code
    FRO
    Advisory Committee
    Unknown
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    FRO Dressing, Wound, Drug

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    Other Clearances by Dumex Medical Surgical Products, Ltd.

    K Number Device Name
    K992732 STERILE WATER & STERILE 0.9% SODIUM CHLORIDE
    K993119 STERILE HYDROGEL
    K990332 DUMEX IODOFORM PACKING STRIP
    K980779 THALAFIX NATURAL SEA SALT DRESSING
    K980861 DUMEX PAK-ITS COTTON GAUZE PACKING IMPREGNATED WITH HYDROGEL
    K980863 DUMEX PAK-ITS NON-WOVEN DRESSING IMPREGNATED SITH SODIUM CHLORIDE (HYPERTONIC)
    K980777 DUMEX PAK-ITS-ABSORBASALT COTTON GAUZE PACKING
    K980791 DUMEX PAK-ITS WOVEN RIBBON PACKING
    K960815 DUPAD, DUPAD W/ABDOM. PAD, DUMEX ABDOM. PAD, COMBO DRESSING ROLL/COMBINE DRESSING ROLL
    K946326 DUTEX GAUZE BANDAGE
    Search all 13 clearances from Dumex Medical Surgical Products, Ltd. →