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FEDERAL REGISTER · NOTICESeptember 29, 2023NOTICE — NO LEGAL EFFECT

Antimicrobial Susceptibility Test System Devices-Updating Breakpoints in Device Labeling; Guidance for Industry; Availability

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Document details are published in the U.S. Federal Register; SPEQ surfaces them for reference and is not affiliated with or endorsed by the FDA or the Office of the Federal Register. The authoritative text is on federalregister.gov.

STATUSNOTICE — NO LEGAL EFFECT
EFFECTIVE—
COMMENTS CLOSE—
APPLIES TO · SPEQ TAGDevice
Document type
Notice
Agency
Health and Human Services Department
Published
September 29, 2023
Document number
2023-21407
Docket
FDA-2023-D-4045
ABSTRACT

The Food and Drug Administration (FDA or we) is announcing the availability of a final guidance for industry and FDA staff entitled "Antimicrobial Susceptibility Test (AST) System Devices--Updating Breakpoints in Device Labeling." This guidance is intended to provide industry and FDA staff with information regarding updating susceptibility test interpretative criteria (STIC)/breakpoints and associated performance data in device labeling for antimicrobial susceptibility test (AST) system devices in response to breakpoint changes posted on the FDA-Recognized Antimicrobial Susceptibility Test Interpretative Criteria website (STIC website). This guidance is expected to facilitate the timely adoption of updated breakpoints in AST system devices, which helps to ensure device safety and effectiveness.

Abstract as published in the Federal Register.

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