Qiagen, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Qiagen, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ipsogen JAK2 RGQ PCR Kit
2
Total
1
Cleared
1
Denied
Qiagen, Inc. has 1 FDA 510(k) cleared medical devices. Based in Gernmantown, US.
Historical record: 1 cleared submissions from 2017 to 2018. Primary specialty: Pathology.
Browse the FDA 510(k) cleared devices submitted by Qiagen, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by QIAGEN Manchester, Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Qiagen, Inc.
2 devices