BEUDAMED
    FDA Registration Active 🇺🇸 United States

    QUICKSCREEN OXYCODONE TEST

    Reg #: 2031229 · FEI: 3000719950 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    3
    Establishment Types
    2
    Classifications
    2

    Registration Details

    Registration Name
    PHAMATECH INC.
    Registration Number
    2031229
    FEI Number
    3000719950
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    15175 Innovation Dr
    City
    San Diego
    State
    CA
    ZIP
    92128
    Country
    US

    Regulatory Submissions

    510(k) Number
    K972619

    Owner / Operator

    Firm Name
    PHAMATECH INC.
    Operator Number
    9026390
    Address
    15175 Innovation Drive, --
    City
    San Diego
    State
    CA
    Postal Code
    92128
    Country
    US
    Correspondent
    Tuan H Pham

    Products

    Device Name Product Code
    Enzyme Immunoassay, Opiates DJG
    Fluorometry, Morphine DJJ

    Proprietary Names

    QUICKSCREEN OXYCODONE TEST QUICKSCREEN ONE STEP OPIATE SCREEN ING TEST

    Establishment Types

    Repack or Relabel Medical Device Manufacture Medical Device