BEUDAMED
    FDA 510(k) FDA unclassified Substantially Equivalent for Some Indications 🇺🇸 United States

    IAMIN GEL WOUND DRESSING

    K Number: K953853 · Decision Feb 5, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    51
    Registration Numbers
    51
    Same Product Code
    144
    Applicant Total
    9
    Review Days
    173

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    Basic Information

    Device Name
    IAMIN GEL WOUND DRESSING
    K Number
    K953853
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent for Some Indications
    Applicant
    Procyte Corp.
    Date Received
    August 16, 1995
    Decision Date
    February 5, 1996
    Product Code
    MGQ
    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
    MGQ Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic

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    Other Clearances by Procyte Corp.

    K Number Device Name
    K971612 OSMO/PCA PILLOW WOUND DRESSING
    K972329 OSMOCYTE RA WOUND DRESSING
    K972150 OSMOCYTE ISLAND WOUND DRESSING
    K970153 LAMIN-2 HYDRATING GEL
    K965143 OSMOCYTE WOUND MANAGER SHEET DRESSING
    K965005 IAMIN IMPREGNATED GAUZE DRESSING
    K964468 IAMIN WET DRESSING (COPPER-SALINE)
    K962623 OSMOCYTE ULTRA/PE PILLOW WOUND DRESSING