BEUDAMED
    FDA Registration Active 🇺🇸 United States

    M3870A FR2 AED Pediatric Defibrillation Pads

    Reg #: 3030677 · FEI: 1000524572 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    Philips North America LLC
    Registration Number
    3030677
    FEI Number
    1000524572
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    22100 Bothell Everett Hwy
    City
    Bothell
    State
    WA
    ZIP
    98021
    Country
    US

    Regulatory Submissions

    510(k) Number
    K003819

    Owner / Operator

    Firm Name
    Philips Medical Systems International BV
    Operator Number
    1217116
    Address
    Veenpluis 6
    City
    Best
    State
    NL-NOTA
    Postal Code
    5684PC
    Country
    NL

    Products

    Device Name Product Code
    Automated External Defibrillators (Non-Wearable) MKJ
    Electrode, Electrocardiograph, Multi-Function MLN

    Proprietary Names

    M3870A FR2 AED Pediatric Defibrillation Pads

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility