BEUDAMED
    FDA Registration Active 🇺🇸 United States

    ACTH EIA

    Reg #: 1222302 · FEI: 1000121039 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    American Laboratory Products Company
    Registration Number
    1222302
    FEI Number
    1000121039
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    26 Keewaydin Drive, Unit G
    City
    Salem
    State
    NH
    ZIP
    03079
    Country
    US

    Regulatory Submissions

    510(k) Number
    K982608

    Owner / Operator

    Firm Name
    AMERICAN LABORATORY PRODUCTS CO., LTD.
    Operator Number
    9000664
    Address
    26 KEEWAYDIN DR., BLDG- G
    City
    Salem
    State
    NH
    Postal Code
    03079
    Country
    US
    Correspondent
    James Richard

    Products

    Device Name Product Code
    Radioimmunoassay, Acth CKG

    Proprietary Names

    ACTH EIA Adrenocorticotropic Hormone ELISA (ACTH ELISA)

    Establishment Types

    Repack or Relabel Medical Device