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510(k) Data Aggregation

    K Number
    K994089
    Manufacturer
    Date Cleared
    2000-02-11

    (70 days)

    Product Code
    Regulation Number
    866.1620
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    HardyDisk™ Chloramphenicol Antinuicobial Seusitivity Disks are used for semi-quantiarive in vitro susceptibility testing by the agar diffusion test procedure (Kirby-Bauer) of rapidly growing and ccrtain fastidious bactcrial pathogens. Standardized methods for agar diffusion icsting have been described for Entcrobactcriaccas, Staphylococcus spp., I seudomonas aeruginusu, Acinctobacter spp., Eisteria monocytogenes, Enterococcus spp., other streptococi and, by modified procedures; Huemophilus influcitzae, and streptococci, including Streptococcus рпеитопіав.

    HardyDisk™ Chloranophenicol is indicated for in vitro activity against the Enterobacteriaciae, Staphylococcus spp., Haemophilus spp., and Streptococous spp., including Streptococcus pneumoniae.

    Device Description

    Not Found

    AI/ML Overview

    The provided text is a 510(k) clearance letter from the FDA for a device called "HardyDiskTM Chloramphenicol 30mcg," which is an antimicrobial susceptibility disk. This document does not contain information about acceptance criteria, device performance tables, study details like sample sizes, ground truth establishment, or multi-reader multi-case studies.

    The letter explicitly states that the device is "substantially equivalent" to legally marketed predicate devices. This implies that the device's performance aligns with established standards for such devices, but the specific performance metrics and a detailed study report are not part of this regulatory clearance document.

    Therefore, I cannot fulfill the request for information regarding acceptance criteria, study details, and performance statistics based on the provided text. The document is a regulatory approval letter, not a scientific study report.

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