BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Q-Pad Test System

    Reg #: 3023949424 · FEI: 3023949424 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    4
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    QURASENSE, INC.
    Registration Number
    3023949424
    FEI Number
    3023949424
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    3517 Edison Way, Ste. D
    City
    Menlo Park
    State
    CA
    ZIP
    94025
    Country
    US

    Regulatory Submissions

    510(k) Number
    K231465

    Owner / Operator

    Firm Name
    Qurasense, Inc.
    Operator Number
    10085929
    Address
    3517 Edison Way, Ste. D
    City
    Menlo Park
    State
    CA
    Postal Code
    94025
    Country
    US
    Correspondent
    Brian Weinberg

    Products

    Device Name Product Code
    Assay, Glycosylated Hemoglobin LCP
    Menstrual Blood Collection Device QZG

    Proprietary Names

    Q-Pad Test System A1c Q-Pad Kit Q-Pad Kit Q-Pad Collection Kit

    Establishment Types

    Manufacture Medical Device