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VITEK 2 AST-Gram Negative Imipenem/Relebactam (<0.25/4 - >16/4 ug/ML)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211136
510(k) Type
Traditional
Applicant
Biomerieux, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/2021
Days to Decision
59 days
Submission Type
Summary

VITEK 2 AST-Gram Negative Imipenem/Relebactam (<0.25/4 - >16/4 ug/ML)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211136
510(k) Type
Traditional
Applicant
Biomerieux, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/2021
Days to Decision
59 days
Submission Type
Summary