QMV — Device To Detect And Identify Selected Microbial Agents That Cause Acute Febrile Illness Class II
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-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K243463 | biofire diagnostics, llc (biomerieux) | BIOFIRE FILMARRAY Tropical Fever Panel | December 5, 2024 |
| K220870 | biofire defense | BioFire Global Fever Panel, BIOFIRE SHIELD Control Kit for the BioFire Global Fe | October 20, 2022 |
| DEN200043 | biofire defense | FilmArray Global Fever Panel | November 20, 2020 |