FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

XPERT MTB/RIF ASSAY

K Number: DEN130032 · Decision Jul 25, 2013
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
1
Applicant Total
50
Review Days
44

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Basic Information

Device Name
XPERT MTB/RIF ASSAY
K Number
DEN130032
Device Class
FDA class 2
Clearance Type
Direct
Regulation Number
866.3373
Medical Specialty
Microbiology
Decision
Unknown
Applicant
Cepheid
Date Received
June 11, 2013
Decision Date
July 25, 2013
Product Code
PEU
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
PEU System, Nucleic Acid-Based, Mycobacterium Tuberculosis Complex, Resistance Marker, Direct Specimen

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K231381 Xpert Xpress MVP; GeneXpert Xpress System
K222638 Xpert® Xpress GBS, GeneXpert® Dx System, GeneXpert® Infinity Systems
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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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