Medical Device Manufacturer · US , Gernmantown , MD

Qiagen, Inc. - FDA 510(k) Cleared Devices

2 submissions · 1 cleared · Since 2017
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.

FDA 510(k) Regulatory Record - Qiagen, Inc.
2 devices
1-2 of 2
Cleared Jan 12, 2018
ipsogen JAK2 RGQ PCR Kit
K172287 · PSU
Pathology · 168d
Not Cleared Mar 27, 2017
ipsogen JAK2 RGQ PCR Kit
DEN160028 · PSU
Pathology · 269d
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