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510(k) Data Aggregation

    K Number
    K021356
    Date Cleared
    2002-07-16

    (78 days)

    Product Code
    Regulation Number
    884.5400
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Applicant Name (Manufacturer) :

    DIVA INTERNATIONAL INC

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    This menstrual cup has the same intended use as the predicate menstrual cup. The DivaCup™ is intended to be used as a receptacle, which is placed in the vagina to collect menstrual flow.

    Device Description

    Not Found

    AI/ML Overview

    I am sorry, but the provided text does not contain information about the acceptance criteria or a study that proves a device meets those criteria. The document is an FDA letter to a company, Diva International, Inc., regarding the 510(k) premarket notification for "The DivaCup Menstrual Solution."

    The letter primarily discusses:

    • The FDA's determination of substantial equivalence for the device.
    • Classification of the device (Class II, Menstrual cup).
    • Applicable regulations and general controls.
    • Contact information for various FDA offices.
    • An "Indications For Use" statement for The DivaCup, which states it "has the same intended use as the predicate menstrual cup" and "is intended to be used as a receptacle, which is placed in the vagina to collect menstrual flow."

    There is no mention of specific performance metrics, acceptance criteria, study methodologies, sample sizes for training or test sets, expert qualifications, ground truth establishment, or any comparative effectiveness studies (e.g., MRMC studies).

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