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510(k) Data Aggregation

    K Number
    K971546
    Date Cleared
    1997-07-10

    (73 days)

    Product Code
    Regulation Number
    880.5100
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    SOMA 900 TRANSPORT BED

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

    The Soma™ Safe Transport Bed is to be used for the management of patients who are excessive in size and those who are the most difficult to care for. The use of this device will assure the prevention of personal injury to the patient and staff.

    Device Description

    Soma 900 Transport Bed

    AI/ML Overview

    I apologize, but the provided text from the FDA 510(k) K971546 approval letter for the "Soma 900 Transport Bed" (later referred to as "Soma Safe Transport Bed") does not contain information regarding acceptance criteria, device performance studies, sample sizes, ground truth establishment, or expert qualifications.

    This document is a regulatory approval letter, specifically a "substantially equivalent" determination letter, which indicates the device can be marketed. It refers to the "indications for use" but does not detail the technical performance studies that would have been submitted as part of the 510(k) application.

    Therefore, I cannot extract the information required to populate the table and answer the subsequent questions about acceptance criteria and the study that proves the device meets them from the provided text. The document focuses on regulatory compliance and approval, not on the technical performance data.

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