BEUDAMED
    FDA Registration Active 🇺🇸 United States

    86000 - VerifyNow Instrument

    Reg #: 3002721930 · FEI: 2250033 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    11
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Accriva Diagnostics, Inc.
    Registration Number
    3002721930
    FEI Number
    2250033
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    6260 Sequence Drive
    City
    San Diego
    State
    CA
    ZIP
    92121
    Country
    US

    Regulatory Submissions

    510(k) Number
    K992531

    Owner / Operator

    Firm Name
    Accriva Diagnostics, Inc.
    Operator Number
    10048042
    Address
    6260 Sequence Drive
    City
    San Diego
    State
    CA
    Postal Code
    92121
    Country
    US
    Correspondent
    Paula Morgan

    Products

    Device Name Product Code
    System, Automated Platelet Aggregation JOZ

    Proprietary Names

    86000 - VerifyNow Instrument 86000D - VerifyNow Instrument 86000L - VerifyNow Instrument 70068 - EQC 85062 - Preventative Maintenance Kit 86003D - VerifyNow Instrument 85063 - Validation Kit 86003L - VerifyNow Instrument 85047 - WQC 86003 - VerifyNow Instrument 86000RF - VerifyNow Instrument

    Establishment Types

    Manufacture Medical Device