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

    STERILE WET DRESSING PACK

    K Number: K781322 · Decision Aug 17, 1978
    View on FDA
    Classifications
    1
    FEI Numbers
    59
    Registration Numbers
    59
    Same Product Code
    270
    Applicant Total
    7
    Review Days
    17

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    Basic Information

    Device Name
    STERILE WET DRESSING PACK
    K Number
    K781322
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Applicant
    W.G. Whitney Corp.
    Date Received
    July 31, 1978
    Decision Date
    August 17, 1978
    Product Code
    EFQ
    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
    EFQ Gauze/Sponge, Internal

    Similar 510(k) Clearances

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    CROSSTEX NON-WOVEN SPONGES

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    GAUZE, SPONGES, CAT # 11-003

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    FDA Unclassified ·Unknown
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    Other Clearances by W.G. Whitney Corp.

    K Number Device Name
    K834532 STERILE WET DRESSING PACK
    K813535 XEROFORM DRESSING
    K810406 STERILE WET DRESSING PACK
    K803299 COLD/HOT PACK
    K800907 TOMAC WET DRESSING WARMER
    K770387 UNICATCH