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510(k) Data Aggregation

    K Number
    K053212
    Device Name
    RAVEN PROPACT
    Date Cleared
    2006-02-15

    (91 days)

    Product Code
    Regulation Number
    880.2800
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    RAVEN PROPACT

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

    The Raven Pro-PACT Peracetic Acid Culture Test Kit is intended for use in testing the efficacy of Steris System1 TM , a liquid chemical sterilization system, processing cycles. A reduced incubation time of 24 hours has been validated for the Raven Pro-PACT Peracetic Acid Culture Test Kit.

    Device Description

    Not Found

    AI/ML Overview

    The provided document is a 510(k) clearance letter from the FDA for a medical device called the "Raven Pro-PACT Peracetic Acid Culture Test Kit." While it confirms the device's substantial equivalence and outlines its indications for use, it does not contain the detailed acceptance criteria or the study data that would prove the device meets those criteria.

    Therefore, I cannot provide the requested information based on the given text.

    The document essentially states:

    • Device Name: Raven Pro-PACT Peracetic Acid Culture Test Kit
    • Intended Use: Testing the efficacy of Steris System1™ liquid chemical sterilization system processing cycles.
    • Key Validation Point: "A reduced incubation time of 24 hours has been validated for the Raven Pro-PACT Peracetic Acid Culture Test Kit."

    To answer your questions, I would need access to the actual 510(k) submission (which often includes performance data and study summaries) or a more detailed technical document about the device's validation.

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