FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

XTAG RESPIRATORY VIRAL PANEL

K Number: K081483 · Decision Jun 25, 2008
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
78
Applicant Total
26
Review Days
28

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
XTAG RESPIRATORY VIRAL PANEL
K Number
K081483
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
866.3980
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Luminex Molecular Diagnostics, Inc.
Date Received
May 28, 2008
Decision Date
June 25, 2008
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OCC), ordered by most recent decision date.

View all

Other Clearances by Luminex Molecular Diagnostics, Inc.

K Number Device Name
K242613 NxTAG® Respiratory Pathogen Panel
K231758 NxTAG Respiratory Pathogen Panel v2 (NxTAG RPP v2)
K193167 NxTAG Respiratory Pathogen Panel, NxTAG Respiratory Pathogen Panel Files, SYNCT Software
K191161 xTAG Gastrointestinal Pathogen Panel (GPP)
K191160 xTAG Gastrointestinal Pathogen Panel (GPP), xTAG Data Analysis Software (TDAS GPP)
K183023 xTAG Gastrointestinal Pathogen Panel (GPP), xTAG Data Analysis Software (TDAS GPP)
K183030 xTAG Gastrointestinal Pathogen Panel (GPP), xTAG Data Analysis Software (TDAS GPP)
K170492 xTAG CYP2D6 Kit v3
K163336 xTAG Cystic Fibrosis 60 Kit v2, xTAG Data Analysis Software (TDAS) CFTR
K163347 xTAG Cystic Fibrosis 39 Kit v2
Search all 26 clearances from Luminex Molecular Diagnostics, Inc. →