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ARTUS INFL A/B RG RT-PCR KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113323
510(k) Type
Traditional
Applicant
QIAGEN GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/6/2012
Days to Decision
88 days
Submission Type
Summary

ARTUS INFL A/B RG RT-PCR KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113323
510(k) Type
Traditional
Applicant
QIAGEN GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/6/2012
Days to Decision
88 days
Submission Type
Summary