BEUDAMED
    Product Code: NKW FDA class 2 21 CFR 870.1670

    Actuator, Syringe, For Injector, Reprocessed

    Cardiovascular

    The Reprocessed Syringe Actuator for Injectors is a reprocessed cardiovascular accessory device that mechanically drives a syringe in an automatic contrast injection system; reprocessing validation data must be included in a 510(k) submission. It is classified as FDA Class 2 (Special Controls), requiring 510(k) clearance, under product code NKW and regulation 21 CFR 870.1670 in the Cardiovascular specialty. The device is eligible for third-party review and is not an implant or life-sustaining device.

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    510(k)s
    0
    FEI Numbers
    0
    Registration Numbers
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    Unique Applicants
    0
    Years Active
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    Basic Information

    Product Code
    NKW
    Device Class
    FDA class 2
    Regulation Number
    870.1670
    Medical Specialty
    Cardiovascular
    Review Panel
    CV
    Submission Type
    1

    Device Characteristics

    ✗
    GMP Exempt
    ✗
    Implant
    ✗
    Life Sustain/Support
    ✓
    Third Party
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    Summary Malfunction Reporting

    Definition

    Reprocessing validation data for this device type must be included in a 510(k) submission. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf).