meddevicedb.com FDA Device Reference

FLU OIA A/B TEST KIT

K023556 Class II Traditional
Decision Date
2003-03-27
Sponsor / Applicant
Thermo Biostar, Inc.

Technical Specification

510(k) Submission ID K023556
Product Code PSZ
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3328
Decision Date 2003-03-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLU OIA A/B TEST KIT received FDA 510(k) clearance under submission number K023556, sponsored by Thermo Biostar, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2003-03-27.

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.