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

    PART #860070 ULTRAPAK & #860075 ULTRAPAK

    K Number: K871474 · Decision Aug 10, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    67
    Registration Numbers
    68
    Same Product Code
    1
    Applicant Total
    8
    Review Days
    118

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    Basic Information

    Device Name
    PART #860070 ULTRAPAK & #860075 ULTRAPAK
    K Number
    K871474
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    886.4350
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Applicant
    Medical Technical Products
    Date Received
    April 14, 1987
    Decision Date
    August 10, 1987
    Product Code
    HOC
    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
    HOC Clip, Iris Retractor

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    K940088 MEDICAL TECHNICAL PRODUCTS STANDARD ULTRASONIC HANDPIECE
    K940084 MODEL 2000 OPHTHALMIC SURGICAL SYSTEM
    K910335 MTP TRANSPORT INFUSION PUMP, MODEL NO. MTPLEA
    K905251 MTP TRANSPORT INFUSION PUMP MODEL NO. 1001A
    K904612 I/A-PHACO SYSTEM (IRR./ASPIR./AND PHACO./SYSTEM)
    K871473 PART #860065 IA PAK & PART #860060 IA PAK