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

Xpert Norovirus, GeneXpert Dx Systems (GX-I, GX-11, GX-IV, GX-XVI), GeneXpert Infinity-48 System, GeneXpert Infinity-48s System, GeneXpert Infinity-80 System

K Number: K142501 · Decision Nov 26, 2014
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
37
Applicant Total
50
Review Days
82

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Basic Information

Device Name
Xpert Norovirus, GeneXpert Dx Systems (GX-I, GX-11, GX-IV, GX-XVI), GeneXpert Infinity-48 System, GeneXpert Infinity-48s System, GeneXpert Infinity-80 System
K Number
K142501
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3990
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cepheid
Date Received
September 5, 2014
Decision Date
November 26, 2014
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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Other Clearances by Cepheid

K Number Device Name
K253653 Xpert Hemorrhagic Fever
K251721 Xpert GI Panel
K250218 Xpert® FII & FV
K242071 Xpert Xpress CoV-2/Flu/RSV plus
DEN240016 Xpert HCV; GeneXpert Xpress System
K231381 Xpert Xpress MVP; GeneXpert Xpress System
K222638 Xpert® Xpress GBS, GeneXpert® Dx System, GeneXpert® Infinity Systems
K221160 Xpert Xpress MVP, GeneXpert Dx System, GeneXpert Infinity System
K203429 Xpert GBS LB XC, GeneXpert Dx System, GeneXpert Infinity System
K212213 Xpert Xpress MVP, GeneXpert Dx System, GeneXpert Infinity System
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