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ARIES C. difficile Assay Complete Kit, ARIES C. difficile Assay Protocol File Kit, ARIES C. difficile Assay Kit (24 cassettes), ARIES Stool Resuspension Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171441
510(k) Type
Traditional
Applicant
Luminex Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/2017
Days to Decision
66 days
Submission Type
Summary

ARIES C. difficile Assay Complete Kit, ARIES C. difficile Assay Protocol File Kit, ARIES C. difficile Assay Kit (24 cassettes), ARIES Stool Resuspension Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171441
510(k) Type
Traditional
Applicant
Luminex Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/2017
Days to Decision
66 days
Submission Type
Summary