BEUDAMED
    FDA 510(k) FDA class 1 Unknown 🇮🇱 Israel

    INSTRUMENTS FOR ONE TIME USE/ DISPOSABLE

    K Number: K903962 · Decision Jul 29, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    285
    Registration Numbers
    286
    Same Product Code
    21
    Applicant Total
    2
    Review Days
    335

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    Basic Information

    Device Name
    INSTRUMENTS FOR ONE TIME USE/ DISPOSABLE
    K Number
    K903962
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Unknown
    Applicant
    Apk Technology
    Date Received
    August 28, 1990
    Decision Date
    July 29, 1991
    Product Code
    LRP
    Advisory Committee
    General, Plastic Surgery
    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
    LRP Tray, Surgical

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    Other Clearances by Apk Technology

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