BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Concentriq Dx

    Reg #: 3025774973 · FEI: 3025774973 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    PROSCIA, INC.
    Registration Number
    3025774973
    FEI Number
    3025774973
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1700 Market St Fl 24
    City
    Philadelphia
    State
    PA
    ZIP
    19103
    Country
    US

    Regulatory Submissions

    510(k) Number
    K230839

    Owner / Operator

    Firm Name
    Proscia, Inc.
    Operator Number
    10060244
    Address
    1700 Market Street, 24th Floor
    City
    Philadelphia
    State
    PA
    Postal Code
    19103
    Country
    US
    Correspondent
    Ian Cadieux

    Products

    Device Name Product Code
    Whole Slide Imaging System PSY
    Digital Pathology Image Viewing And Management Software QKQ

    Proprietary Names

    Concentriq Dx Concentriq AP-Dx-US Concentriq AP-Dx

    Establishment Types

    Manufacture Medical Device