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

FilmArray Blood Culture Identification (BCID) panel for use with FilmArray Torch

K Number: K160457 · Decision Mar 15, 2016
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
10
Applicant Total
28
Review Days
25

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Basic Information

Device Name
FilmArray Blood Culture Identification (BCID) panel for use with FilmArray Torch
K Number
K160457
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
866.3365
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biofire Diagnostics, LLC
Date Received
February 19, 2016
Decision Date
March 15, 2016
Product Code
PEN
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
PEN Gram-Negative Bacteria And Associated Resistance Markers

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K242367 BIOFIRE FILMARRAY Gastrointestinal (GI) Panel
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K230719 BIOFIRE® SPOTFIRE® Respiratory (R) Panel Mini
K230404 BIOFIRE FILMARRAY Gastrointestinal (GI) Panel
K222601 FilmArray Pneumonia Panel plus
DEN200066 BioFire Joint Infection (JI) Panel
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