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

    Silatrix Oral Gel

    K Number: K202000 · Decision Nov 20, 2020
    View on FDA
    Classifications
    1
    FEI Numbers
    31
    Registration Numbers
    31
    Same Product Code
    40
    Applicant Total
    2
    Review Days
    123

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    Basic Information

    Device Name
    Silatrix Oral Gel
    K Number
    K202000
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Sa3, LLC
    Date Received
    July 20, 2020
    Decision Date
    November 20, 2020
    Product Code
    OLR
    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
    OLR Oral Wound Dressing

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    Other Clearances by Sa3, LLC

    K Number Device Name
    K252425 Silatrix Oral Gel