meddevicedb.com FDA Device Reference

TRU FLU

K133714 Class II Special
Decision Date
2014-01-03
Sponsor / Applicant
Meridian Bioscience, Inc.

Technical Specification

510(k) Submission ID K133714
Product Code PSZ
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3328
Decision Date 2014-01-03
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRU FLU received FDA 510(k) clearance under submission number K133714, sponsored by Meridian Bioscience, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2014-01-03.

Classification & Regulation

This clearance is catalogued under FDA product code PSZ and 21 CFR 866.3328, within the Microbiology review panel as a Class II device.