Last synced on 30 May 2025 at 11:05 pm

illumigene Pertussis DNA Amplification Assay

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152285
510(k) Type
Traditional
Applicant
MERIDIAN BIOSCIENCE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/2015
Days to Decision
90 days
Submission Type
Statement

illumigene Pertussis DNA Amplification Assay

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152285
510(k) Type
Traditional
Applicant
MERIDIAN BIOSCIENCE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/2015
Days to Decision
90 days
Submission Type
Statement