ClearanceBrief
510(k) K140407 ยท PCH Gastrointestinal Pathogen Panel Multiplex Nucleic Acid-Based Assay System

FILMARRAY GASTROINTESTINAL (GI) PANEL

ApplicantBiofire Diagnostics, Salt Lake City UT, US
DecisionSubstantially Equivalent, May 2, 2014
ReceivedFeb 18, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K140407

DateFirm and productCodeLinked 510(k)
Sep 30, 2024BioFire Diagnostics, LLC
FILMARRAY Gastrointestinal (GI) Panel (Part No.: RFIT-ASY-0104 & RFIT-ASY-0116) Pouch Module Software
Open, Classified
PCHNone listed
Aug 6, 2024BioFire Diagnostics, LLC
BIOFIRE FILMARRAY Gastrointestinal (GI) Panel REF RFIT-ASY-0116 (30 test kit) BIOFIRE FILMARRAY Gastrointestinal (GI) Panel REF RFIT-ASY-0104 (6 kit test) The BIOFIRE FILMARRAY Gastrointestinal (GI
Open, Classified
PCHNone listed
Feb 15, 2024BioFire Diagnostics, LLC
FilmArray Gastrointestinal (GI) Panel RFIT-ASY-0116 (30 test kit) RFIT-ASY-0104 (6 test kit) Gastrointestinal microorganism multiplex nucleic acid-based assay. In vitro diagnostic.
Open, Classified
PCHNone listed
Jan 10, 2024BioFire Diagnostics, LLC
BIOFIRE FILMARRAY Gastrointestinal (GI) Panel is a qualitative multiplexed nucleic acid-based in vitro diagnostic test intended for use with BIOFIRE FILMARRAY Systems.
Open, Classified
PCHNone listed
Apr 14, 2023BioFire Diagnostics, LLC
FilmArray Gastrointestinal (GI) Panel for FILMARRAY Systems, REF: RFIT-ASY-0116, (30 pouches/kit)
Open, Classified
PCHNone listed
Mar 15, 2023BioFire Diagnostics, LLC
In Vitro Diagnostic (IVD) Panel FilmArray GI Panel - REF RFIT-ASY-0116
Open, Classified
PCHNone listed
Aug 8, 2019BioFire Diagnostics, LLC
FilmArray Gastronintestinal (GI) Panel, REF: RFIT-ASY-0104, 6-pack kit, UDI (01)00815381020116, CE IVD, Rx Only
Terminated
PCHNone listed
Mar 6, 2019BioFire Diagnostics, LLC
FilmArray Gastrointestinal (GI) Panel, IVD, Rx Only, Biofire Diagnostics, LLC REF: RFIT-ASY-0104, and RFIT-ASY-0116), Product Usage: The FilmArray Gastrointestinal (GI) Panel is a qualitative multip
Terminated
PCHNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.