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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
FDA Hosted 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
FDA Hosted 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