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ETEST Imipenem/Relebactam (IPR) (0.002/4-32/4 ug/mL)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191953
510(k) Type
Traditional
Applicant
Biomerieux S.A.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
8/22/2019
Days to Decision
31 days
Submission Type
Summary

ETEST Imipenem/Relebactam (IPR) (0.002/4-32/4 ug/mL)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191953
510(k) Type
Traditional
Applicant
Biomerieux S.A.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
8/22/2019
Days to Decision
31 days
Submission Type
Summary