BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    SCISSORS, STRABIMUS, 4 STRAIGHT

    K Number: K770040 · Decision Jan 14, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    261
    Registration Numbers
    261
    Same Product Code
    14
    Applicant Total
    18
    Review Days
    4

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    Basic Information

    Device Name
    SCISSORS, STRABIMUS, 4 STRAIGHT
    K Number
    K770040
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    886.4350
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Applicant
    J. Sklar Mfg. Co., Inc.
    Date Received
    January 10, 1977
    Decision Date
    January 14, 1977
    Product Code
    HNF
    Advisory Committee
    Ophthalmic
    Review Advisory Committee
    OP
    Third Party
    N

    Classifications

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

    Product Code Device Name
    HNF Scissors, Ophthalmic

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