FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

BIOFIRE SPOTFIRE Respiratory/Sore Throat (R/ST) Panel Mini

K Number: K241194 · Decision May 30, 2024
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
32
Applicant Total
28
Review Days
30

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Basic Information

Device Name
BIOFIRE SPOTFIRE Respiratory/Sore Throat (R/ST) Panel Mini
K Number
K241194
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
866.3981
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biofire Diagnostics, LLC
Date Received
April 30, 2024
Decision Date
May 30, 2024
Product Code
QOF
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
QOF Multi-Target Respiratory Specimen Nucleic Acid Test Including Sars-Cov-2 And Other Microbial Agents

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Other Clearances by Biofire Diagnostics, LLC

K Number Device Name
K243544 BIOFIRE SPOTFIRE Respiratory/Sore Throat Panel Mini
K243885 BIOFIRE FILMARRAY Gastrointestinal (GI) Panel Mid
K243759 BIOFIRE Blood Culture Identification 2 (BCID2) Panel (RFIT-ASY-0147 (30 pack) RFIT-ASY-0148 (6 pack))
K242367 BIOFIRE FILMARRAY Gastrointestinal (GI) Panel
K232954 BIOFIRE SPOTFIRE Respiratory/Sore Throat (R/ST) Panel
K230719 BIOFIRE® SPOTFIRE® Respiratory (R) Panel Mini
K230404 BIOFIRE FILMARRAY Gastrointestinal (GI) Panel
K222601 FilmArray Pneumonia Panel plus
DEN200066 BioFire Joint Infection (JI) Panel
K212727 FilmArray Pneumonia Panel
Search all 28 clearances from Biofire Diagnostics, LLC →