Last synced on 14 November 2025 at 11:06 pm

Xpert CT/NG, GeneXpert Dx System, GeneXpert Infinity-48s and GeneXpert Infinity-80 Systems, GeneXpert Infinity-48 System, Xpert Vaginal/Endocervical Specimen Collection, Xpert Urine Specimen Collection Kit, Xpert Swab Specimen Collection Kit

Page Type
Cleared 510(K)
510(k) Number
K190441
510(k) Type
Traditional
Applicant
Cepheid
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2019
Days to Decision
87 days
Submission Type
Summary

Xpert CT/NG, GeneXpert Dx System, GeneXpert Infinity-48s and GeneXpert Infinity-80 Systems, GeneXpert Infinity-48 System, Xpert Vaginal/Endocervical Specimen Collection, Xpert Urine Specimen Collection Kit, Xpert Swab Specimen Collection Kit

Page Type
Cleared 510(K)
510(k) Number
K190441
510(k) Type
Traditional
Applicant
Cepheid
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2019
Days to Decision
87 days
Submission Type
Summary