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510(k) Data Aggregation

    K Number
    K964396
    Date Cleared
    1997-06-06

    (214 days)

    Product Code
    Regulation Number
    884.5160
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The Double Up Breast Pump is indicated to facilitate expression of milk from the breasts of lactating women

    Device Description

    Double Up Breast Pump

    AI/ML Overview

    The provided document is a 510(k) Pre-Market Notification letter from the FDA regarding the "Double Up Breast Pump." This letter indicates that the device has been found substantially equivalent to a predicate device and can be marketed.

    However, this document does not contain any information about acceptance criteria, performance studies, sample sizes, expert qualifications, ground truth, or adjudication methods. The 510(k) clearance process sometimes relies on demonstrating substantial equivalence to a legally marketed predicate device, rather than requiring new clinical performance studies that would typically include the details you've requested.

    Therefore, I cannot fulfill your request for the specific details about acceptance criteria and the study proving the device meets them based solely on the provided text. The document is primarily a regulatory approval letter.

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