The following data is part of a premarket notification filed by Luminex Molecular Diagnostics, Inc. with the FDA for Xtag Gastrointestinal Pathogen Panel(gpp)/xtag Data Analysis Software For Gpp(tdas Gpp).
Device ID | K140647 |
510k Number | K140647 |
Device Name: | XTAG GASTROINTESTINAL PATHOGEN PANEL(GPP)/XTAG DATA ANALYSIS SOFTWARE FOR GPP(TDAS GPP) |
Classification | Gastrointestinal Pathogen Panel Multiplex Nucleic Acid-based Assay System |
Applicant | LUMINEX MOLECULAR DIAGNOSTICS, INC. 439 UNIVERSITY AVE. Toronto, Ontario, CA M5g 1y8 |
Contact | Tina Ip |
Correspondent | Tina Ip LUMINEX MOLECULAR DIAGNOSTICS, INC. 439 UNIVERSITY AVE. Toronto, Ontario, CA M5g 1y8 |
Product Code | PCH |
CFR Regulation Number | 866.3990 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-03-13 |
Decision Date | 2014-10-24 |
Summary: | summary |