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FILMARRAY BLOOD CULTURE IDENTIFICATION (BCID) PANEL

K130914 Class II Traditional
Decision Date
2013-06-21
Sponsor / Applicant
Biofire Diagnostics, Inc.

Technical Specification

510(k) Submission ID K130914
Product Code PEN
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3365
Decision Date 2013-06-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FILMARRAY BLOOD CULTURE IDENTIFICATION (BCID) PANEL received FDA 510(k) clearance under submission number K130914, sponsored by Biofire Diagnostics, 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 2013-06-21.

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.