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

    DISPOSABLE ECG MONITORING ELECTRODES, MODELS 4500,4530, 4533, 4539, 4540, AND 4560

    K Number: K990113 · Decision Dec 6, 1999
    View on FDA
    Classifications
    1
    FEI Numbers
    191
    Registration Numbers
    191
    Same Product Code
    328
    Applicant Total
    9
    Review Days
    327

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    Basic Information

    Device Name
    DISPOSABLE ECG MONITORING ELECTRODES, MODELS 4500,4530, 4533, 4539, 4540, AND 4560
    K Number
    K990113
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2360
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Maersk Medical A/S
    Date Received
    January 13, 1999
    Decision Date
    December 6, 1999
    Product Code
    DRX
    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
    DRX Electrode, Electrocardiograph

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    Other Clearances by Maersk Medical A/S

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    K990112 DISPOSABLE ECG MONITORING ELECTRODES, MODELS 4060, 4610
    K990110 DISPOSABLE ECG MONITORING ELECTRODES, MODEL 4110, 4140
    K990111 DISPOSABLE ECG MONITORING ELECTRODES, MODELS 4520, 4535, 4570
    K990115 DISPOSABLE ECG MONITORING ELECTRODES, MODELS, 4420, 4440
    K991759 MAERSK MEDICAL CONTOUR INFUSION SET
    K973364 4L DRAINAGE BAG, 4L BAG FOR PERITONEAL DIALYSIS, 4L URINARY DRAINAGE BAG