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

FilmArray Respiratory Panel 2 (RP2)

K Number: K170604 · Decision May 30, 2017
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
78
Applicant Total
28
Review Days
90

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Basic Information

Device Name
FilmArray Respiratory Panel 2 (RP2)
K Number
K170604
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3980
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biofire Diagnostics, LLC
Date Received
March 1, 2017
Decision Date
May 30, 2017
Product Code
OCC
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
OCC Respiratory Virus Panel Nucleic Acid Assay System

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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
K241194 BIOFIRE SPOTFIRE Respiratory/Sore Throat (R/ST) Panel Mini
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
Search all 28 clearances from Biofire Diagnostics, LLC →