K Number
K192326
Manufacturer
Date Cleared
2019-09-19

(23 days)

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

Not Found

Device Description

Not Found

AI/ML Overview

The provided text is an FDA clearance letter for a medical device (HardyDisk AST Lefamulin 20μg). It does not contain information about acceptance criteria, device performance, study details, sample sizes, expert qualifications, ground truth establishment, or any of the specific technical details requested in the prompt.

Therefore, I cannot fulfill the request using only the provided text. To answer your questions, I would need a different document, such as a study report, 510(k) summary, or a more detailed technical description of the device's performance characteristics.

§ 866.1620 Antimicrobial susceptibility test disc.

(a)
Identification. An antimicrobial susceptibility test disc is a device that consists of antimicrobic-impregnated paper discs used to measure by a disc-agar diffusion technique or a disc-broth elution technique the in vitro susceptibility of most clinically important bacterial pathogens to antimicrobial agents. In the disc-agar diffusion technique, bacterial susceptibility is ascertained by directly measuring the magnitude of a zone of bacterial inhibition around the disc on an agar surface. The disc-broth elution technique is associated with an automated rapid susceptibility test system and employs a fluid medium in which susceptibility is ascertained by photometrically measuring changes in bacterial growth resulting when antimicrobial material is eluted from the disc into the fluid medium. Test results are used to determine the antimicrobial agent of choice in the treatment of bacterial diseases.(b)
Classification. Class II (performance standards).