Last synced on 25 January 2026 at 3:41 am

VITEK MS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN130013
510(k) Type
Direct
Applicant
Biomerieux, Inc.
Country
United States
FDA Decision
Deleted
Decision Date
8/21/2013
Days to Decision
231 days

VITEK MS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN130013
510(k) Type
Direct
Applicant
Biomerieux, Inc.
Country
United States
FDA Decision
Deleted
Decision Date
8/21/2013
Days to Decision
231 days