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

FilmArray Gastrointestinal (GI) Panel for use with the FilmArray 2.0

K Number: K143005 · Decision Feb 19, 2015
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
37
Applicant Total
28
Review Days
122

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Basic Information

Device Name
FilmArray Gastrointestinal (GI) Panel for use with the FilmArray 2.0
K Number
K143005
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3990
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biofire Diagnostics, LLC
Date Received
October 20, 2014
Decision Date
February 19, 2015
Product Code
PCH
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
PCH Gastrointestinal Pathogen Panel Multiplex Nucleic Acid-Based Assay System

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