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Xpert® TV Assay on the Cepheid GeneXpert Instrument Systems (GeneXpert Dx, GeneXpert Infinity-48, GeneXpert Infinity-48s, and GeneXpertInfinity-80 systems), Xpert Vaginal/Endocervical Specimen Collection Kit, and Xpert Urine Specimen Collection Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151565
510(k) Type
Traditional
Applicant
CEPHEID
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/2015
Days to Decision
128 days
Submission Type
Summary

Xpert® TV Assay on the Cepheid GeneXpert Instrument Systems (GeneXpert Dx, GeneXpert Infinity-48, GeneXpert Infinity-48s, and GeneXpertInfinity-80 systems), Xpert Vaginal/Endocervical Specimen Collection Kit, and Xpert Urine Specimen Collection Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151565
510(k) Type
Traditional
Applicant
CEPHEID
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/2015
Days to Decision
128 days
Submission Type
Summary