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510(k) Data Aggregation

    K Number
    K982215

    Validate with FDA (Live)

    Date Cleared
    1998-09-18

    (87 days)

    Product Code
    Regulation Number
    868.5915
    Age Range
    All
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Manual ventilation and assist in verification of endotracheal tube placement

    Device Description

    Manual Resuscitator with ACE

    AI/ML Overview

    I am sorry, but the provided text from the FDA document (K982215) is a letter regarding the substantial equivalence determination for a "Manual Resuscitator with ACE" device. It does not contain any information about acceptance criteria, study data, sample sizes, ground truth establishment, or any performance metrics for the device.

    Therefore, I cannot fulfill your request to describe the acceptance criteria and the study that proves the device meets them based on the given information. The document is a regulatory approval letter, not a scientific study report.

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    K Number
    K961867

    Validate with FDA (Live)

    Device Name
    PEEP VALVE
    Date Cleared
    1996-08-13

    (90 days)

    Product Code
    Regulation Number
    868.5965
    Age Range
    N/A
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use
    Device Description
    AI/ML Overview
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    K Number
    K961330

    Validate with FDA (Live)

    Date Cleared
    1996-07-02

    (85 days)

    Product Code
    Regulation Number
    868.5915
    Age Range
    N/A
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use
    Device Description
    AI/ML Overview
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    K Number
    K961329

    Validate with FDA (Live)

    Date Cleared
    1996-07-02

    (85 days)

    Product Code
    Regulation Number
    868.5915
    Age Range
    N/A
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use
    Device Description
    AI/ML Overview
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    K Number
    K961332

    Validate with FDA (Live)

    Date Cleared
    1996-06-28

    (81 days)

    Product Code
    Regulation Number
    868.5915
    Age Range
    N/A
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use
    Device Description
    AI/ML Overview
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    K Number
    K961369

    Validate with FDA (Live)

    Date Cleared
    1996-06-28

    (80 days)

    Product Code
    Regulation Number
    868.5915
    Age Range
    N/A
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use
    Device Description
    AI/ML Overview
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    K Number
    K961868

    Validate with FDA (Live)

    Date Cleared
    1996-06-28

    (44 days)

    Product Code
    Regulation Number
    868.5915
    Age Range
    N/A
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use
    Device Description
    AI/ML Overview
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    K Number
    K961882

    Validate with FDA (Live)

    Date Cleared
    1996-06-28

    (44 days)

    Product Code
    Regulation Number
    868.5915
    Age Range
    N/A
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use
    Device Description
    AI/ML Overview
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    K Number
    K961331

    Validate with FDA (Live)

    Date Cleared
    1996-06-28

    (81 days)

    Product Code
    Regulation Number
    868.5915
    Age Range
    N/A
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use
    Device Description
    AI/ML Overview
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    K Number
    K953546

    Validate with FDA (Live)

    Date Cleared
    1996-02-29

    (216 days)

    Product Code
    Regulation Number
    868.5915
    Age Range
    N/A
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use
    Device Description
    AI/ML Overview
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