BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    Propeller Sensor for Neohaler

    K Number: K180770 · Decision Aug 1, 2018
    View on FDA
    Classifications
    1
    FEI Numbers
    189
    Registration Numbers
    189
    Same Product Code
    507
    Applicant Total
    6
    Review Days
    131

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    Basic Information

    Device Name
    Propeller Sensor for Neohaler
    K Number
    K180770
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5630
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Reciprocal Labs Corporation
    Date Received
    March 23, 2018
    Decision Date
    August 1, 2018
    Product Code
    CAF
    Advisory Committee
    Anesthesiology
    Review Advisory Committee
    AN
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    CAF Nebulizer (Direct Patient Interface)

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    Other Clearances by Reciprocal Labs Corporation

    K Number Device Name
    K192724 Propeller Sensor for Symbicort
    K161454 Propeller Sensor Model 2015-E
    K142516 Propeller System
    K140638 PROPELLER SYSTEM - MODEL 2
    K121609 ASTHMAPOLIS SYSTEM