Last synced on 2 May 2025 at 11:05 pm

Revogene

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243922
510(k) Type
Traditional
Applicant
Meridian Bioscience, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/2025
Days to Decision
90 days
Submission Type
Summary

Revogene

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243922
510(k) Type
Traditional
Applicant
Meridian Bioscience, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/2025
Days to Decision
90 days
Submission Type
Summary