BEUDAMED
    FDA Registration Active 🇺🇸 United States

    3M™ Littmann® CORE Digital Stethoscope

    Reg #: 3011651230 · FEI: 3011651230 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Eko Health, Inc.
    Registration Number
    3011651230
    FEI Number
    3011651230
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    2100 Powell St, Suite 300
    City
    Emeryville
    State
    CA
    ZIP
    94608
    Country
    US

    Regulatory Submissions

    510(k) Number
    K200776

    Owner / Operator

    Firm Name
    Eko Health, Inc.
    Operator Number
    10049275
    Address
    2100 Powell St, Suite 300
    City
    Emeryville
    State
    CA
    Postal Code
    94608
    Country
    US
    Correspondent
    Connor Landgraf

    Products

    Device Name Product Code
    Stethoscope, Electronic DQD

    Proprietary Names

    3M™ Littmann® CORE Digital Stethoscope Eko CORE SENSORA

    Establishment Types

    Manufacture Medical Device