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510(k) Data Aggregation

    K Number
    K173873
    Date Cleared
    2018-03-16

    (86 days)

    Product Code
    Regulation Number
    866.2560
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    BD BACTEC Peds Plus/F Culture Vials Soybean-Casein Digest Broth with Resins in a Plastic Vial

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

    BD BACTEC Peds Plus™F culture vials (enriched Soybean-Casein Digest broth with CO2) are for aerobic blood cultures. Principal use is with the BD BACTEC fluorescent series instruments for the qualitative culture and recovery of aerobic microorganisms (mainly bacteria and yeast) from pediatric and non-pediatric blood specimens which are generally less than 3 mL in volume.

    Device Description

    The sample to be tested is inoculated into one or more vials which are inserted into the BD BACTEC fluorescent series instrument for incubation and periodic reading. Each vial contains a chemical sensor which can detect increases in CO2 produced by the growth of microorganisms. The sensor's fluorescence measurement is detected at regular intervals to determine the change in CO2 present in the system. A positive reading indicates the presumptive presence of viable microorganisms in the vial. BD BACTEC Peds Plus™F culture vial detection is limited to microorganisms that will grow in a particular type of medium.

    AI/ML Overview

    The document describes the analytical performance criteria and the study conducted for the BD BACTEC™ Peds Plus™/F Culture Vials.

    Here's the breakdown of the information requested:

    1. Table of Acceptance Criteria and Reported Device Performance:

    Acceptance Criteria CategoryAcceptance CriteriaReported Device Performance (BD BACTEC Peds Plus/F Plastic Vial vs. Glass Vial)
    Instrument Time to Detection (TTD)Median TTD difference
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