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Rheonix STI TriPlex Assay, Rheonix EncompassMDx Workstation (instrument and software), Rheonix Urine Specimen Collection Kit

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193081
510(k) Type
Traditional
Applicant
Rheonix, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2021
Days to Decision
773 days
Submission Type
Summary

Rheonix STI TriPlex Assay, Rheonix EncompassMDx Workstation (instrument and software), Rheonix Urine Specimen Collection Kit

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193081
510(k) Type
Traditional
Applicant
Rheonix, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2021
Days to Decision
773 days
Submission Type
Summary