meddevicedb.com FDA Device Reference

HardyDisk AST Rezafungin 5µg (RZF5)

K230827 Class II Traditional
Decision Date
2023-06-01
Sponsor / Applicant
Hardy Diagnostics

Technical Specification

510(k) Submission ID K230827
Product Code JTN
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.1620
Decision Date 2023-06-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HardyDisk AST Rezafungin 5µg (RZF5) received FDA 510(k) clearance under submission number K230827, sponsored by Hardy Diagnostics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2023-06-01.

Classification & Regulation

This clearance is catalogued under FDA product code JTN and 21 CFR 866.1620, within the Microbiology review panel as a Class II device.