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FilmArray Blood Culture Identification (BCID) Panel for use with the FilmArray 2.0

K143171 Class II Traditional
Decision Date
2015-01-30
Sponsor / Applicant
Biofire Diagnostics, LLC

Technical Specification

510(k) Submission ID K143171
Product Code PEN
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3365
Decision Date 2015-01-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FilmArray Blood Culture Identification (BCID) Panel for use with the FilmArray 2.0 received FDA 510(k) clearance under submission number K143171, sponsored by Biofire Diagnostics, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2015-01-30.

Classification & Regulation

This clearance is catalogued under FDA product code PEN and 21 CFR 866.3365, within the Microbiology review panel as a Class II device.