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XPERT FLU/RSV XC ASSAY

K142045 Class II Traditional
Decision Date
2014-11-22
Sponsor / Applicant
Cepheid

Technical Specification

510(k) Submission ID K142045
Product Code OCC
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3980
Decision Date 2014-11-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

XPERT FLU/RSV XC ASSAY received FDA 510(k) clearance under submission number K142045, sponsored by Cepheid. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2014-11-22.

Classification & Regulation

This clearance is catalogued under FDA product code OCC and 21 CFR 866.3980, within the Microbiology review panel as a Class II device.