QMV — Device To Detect And Identify Selected Microbial Agents That Cause Acute Febrile Illness Class II

FDA Device Classification

Classification Details

Product Code
QMV
Device Class
Class II
Regulation Number
866.3966
Submission Type
Review Panel
MI
Medical Specialty
Microbiology
Implant
No

Definition

A device to detect and identify selected microbial agents that cause acute febrile illness is identified as a in vitro device intended for the detection and identification of microbial agents in human clinical specimens from patients with signs and symptoms of acute febrile illness who are at risk for exposure or who may have been exposed to these agents. It is intended to aid in the diagnosis of acute febrile illness in conjunction with other clinical, epidemiologic, and laboratory data, including patient travel, pathogen endemicity, or other risk factors.

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K243463biofire diagnostics, llc (biomerieux)BIOFIRE FILMARRAY Tropical Fever PanelDecember 5, 2024
K220870biofire defenseBioFire Global Fever Panel, BIOFIRE SHIELD Control Kit for the BioFire Global FeOctober 20, 2022
DEN200043biofire defenseFilmArray Global Fever PanelNovember 20, 2020