Luminex Molecular Diagnostics, Inc. - FDA 510(k) Cleared Devices
26
Total
22
Cleared
2
Denied
Luminex Molecular Diagnostics, Inc. has 22 FDA 510(k) cleared medical devices. Based in Toronto, Ontario, CA.
Latest FDA clearance: Oct 2024. Active since 2008. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Luminex Molecular Diagnostics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Luminex Molecular Diagnostics, Inc.
26 devices
Cleared
Oct 02, 2024
NxTAG® Respiratory Pathogen Panel
Microbiology
29d
Cleared
Mar 11, 2024
NxTAG Respiratory Pathogen Panel v2 (NxTAG RPP v2)
Microbiology
269d
Cleared
Dec 11, 2019
NxTAG Respiratory Pathogen Panel, NxTAG Respiratory Pathogen Panel Files,...
Microbiology
26d
Cleared
Nov 12, 2019
xTAG Gastrointestinal Pathogen Panel (GPP)
Microbiology
195d
Cleared
Nov 04, 2019
xTAG Gastrointestinal Pathogen Panel (GPP), xTAG Data Analysis Software (TDAS...
Microbiology
187d
Cleared
Nov 30, 2018
xTAG Gastrointestinal Pathogen Panel (GPP), xTAG Data Analysis Software (TDAS...
Microbiology
29d
Cleared
Nov 30, 2018
xTAG Gastrointestinal Pathogen Panel (GPP), xTAG Data Analysis Software (TDAS...
Microbiology
29d
Cleared
Aug 11, 2017
xTAG CYP2D6 Kit v3
Toxicology
175d
Cleared
Dec 15, 2016
xTAG Cystic Fibrosis 60 Kit v2, xTAG Data Analysis Software (TDAS) CFTR
Medical Genetics
17d
Cleared
Dec 15, 2016
xTAG Cystic Fibrosis 39 Kit v2
Medical Genetics
17d
Cleared
Dec 17, 2015
NxTAG Respiratory Pathogen Panel, NxTAG Respiratory Pathogen Panel Files,...
Microbiology
115d
Cleared
Oct 24, 2014
XTAG GASTROINTESTINAL PATHOGEN PANEL(GPP)/XTAG DATA ANALYSIS SOFTWARE FOR...
Microbiology
225d