Last synced on 6 December 2024 at 11:05 pm

VITEK MS PRIME

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212461
510(k) Type
Traditional
Applicant
bioMerieux, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/2022
Days to Decision
221 days
Submission Type
Summary

VITEK MS PRIME

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212461
510(k) Type
Traditional
Applicant
bioMerieux, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/2022
Days to Decision
221 days
Submission Type
Summary