BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    MICRON, MICROVASCULAR DOPPLER

    K Number: K860651 · Decision Jul 18, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    44
    Registration Numbers
    44
    Same Product Code
    136
    Applicant Total
    3
    Review Days
    147

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    Basic Information

    Device Name
    MICRON, MICROVASCULAR DOPPLER
    K Number
    K860651
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2100
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Diagnostic Electronics Corp.
    Date Received
    February 21, 1986
    Decision Date
    July 18, 1986
    Product Code
    DPW
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DPW Flowmeter, Blood, Cardiovascular

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    Other Clearances by Diagnostic Electronics Corp.

    K Number Device Name
    K861023 DOPPLEX, PULSED/CONTINUOUS WAVE DOPPOLER
    K830628 REAL-TIME SPECTRUM ANALYZER