FDA 510(k) Applications Submitted by QIAGEN, GMBH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K113323 | 11/10/2011 | ARTUS INFL A/B RG RT-PCR KIT | QIAGEN, GMBH |
| K133936 | 12/23/2013 | ARTUS C. DIFFICILE QS-RGQ MDX KIT | QIAGEN, GMBH |
| K113319 | 11/10/2011 | ROTOR-GENE Q MDX | QIAGEN, GMBH |
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