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

    PRO-FECT STERILE GAUZE SPONGES

    K Number: K962227 · Decision Aug 19, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    59
    Registration Numbers
    59
    Same Product Code
    270
    Applicant Total
    1
    Review Days
    70

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    Basic Information

    Device Name
    PRO-FECT STERILE GAUZE SPONGES
    K Number
    K962227
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Network Trading Corp. Dba Grand Intl.
    Date Received
    June 10, 1996
    Decision Date
    August 19, 1996
    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

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