BEUDAMED
    FDA Registration Active 🇺🇸 United States

    NEUWAVE LKXT Ablation Probes

    Reg #: 3008769756 · FEI: 3008769756 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    22
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    NEUWAVE MEDICAL, INC.
    Registration Number
    3008769756
    FEI Number
    3008769756
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    3529, 3513(Suite 100) and 3543 Anderson Street
    City
    Madison
    State
    WI
    ZIP
    53704
    Country
    US

    Regulatory Submissions

    510(k) Number
    K200081

    Owner / Operator

    Firm Name
    NeuWave Medical, Inc.
    Operator Number
    10034016
    Address
    3529 Anderson Street
    City
    Madison
    State
    WI
    Postal Code
    53704
    Country
    US
    Correspondent
    Emily Nesbitt

    Products

    Device Name Product Code
    System, Ablation, Microwave And Accessories NEY

    Proprietary Names

    NEUWAVE LKXT Ablation Probes NEUWAVE Certus LK Ablation Probes Certus 140 2.45GHz Ablation System NEUWAVE PRS Ablation Probes Foot Switch Accessories NEUWAVE SR Ablation Probes NEUWAVE LN Ablation Probes NEUWAVE Certus PR Ablation Probes Certus SR Ablation Probes NEUWAVE PR Ablation Probes NEUWAVE Microwave Ablation System NEUWAVE Certus PRXT Ablation Probes NEUWAVE Certus LKXT Ablation Probes Certus PR Ablation Probes Certus LN Ablation Probes NEUWAVE PRXT Ablation Probes NEUWAVE LK Ablation Probes Certus LK Ablation Probes Certus LKXT Ablation Probes Certus PRXT Ablation Probes Dual Probe Clips NEUWAVE Certus Microwave Ablation System

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device