Qiagen Inc

FDA Filings

This page includes the latest FDA filings for Qiagen Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Filings

Device Company	Device	Date
PMA P160052S001 QIAGEN Inc	PartoSure Test	2019-10-11
PMA P130027S006 QIAGEN, INC.	artus CMV RGQ MDx Kit and artus CMV QS-RGO MDx Kit	2018-09-26
PMA P160052 QIAGEN Inc	PartoSure test	2018-04-11
PMA P130027S005 QIAGEN, INC.	artus CMV RGQ MDx Kit and artus CMV QS_RGQ MDx Kit	2018-04-06
PMA P130027S004 QIAGEN, INC.	artus CMV RGQ MDx Kit and artus CMV QS-RGQ MDx Kit	2018-03-13
PMN K172287 QIAGEN, Inc.	Ipsogen JAK2 RGQ PCR Kit	2018-01-12
PMA P130027S003 QIAGEN, INC.	Artus CMV RGQ and QS-RGQ MDx Kit	2017-11-15
PMA P130027S002 QIAGEN, INC.	ARTUS CMV RGQ MDX KIT	2017-06-02
De Novo DEN160028 QIAGEN INC	Ipsogen JAK2 RGQ PCR Kit	2017-03-27
PMA P130027S001 QIAGEN, INC.	ARTUS CMV RGQ MDX KIT	2015-07-09
PMA P130027 QIAGEN, INC.	ARTUS CMV RGQ MDX KIT	2014-06-02
PMA P880009S005 QIAGEN, INC.	VIRAPAP HUMAN PAPILLOMAVIRUS DNA DETECTION KIT	1993-05-17
PMA P880009S004 QIAGEN, INC.	VIRAPAP HUMAN PAPILLOMAVIRUS DNA DETECTION KIT	1991-08-19
PMA P880009S003 QIAGEN, INC.	VIRAPAP HUMAN PAPILLOMAVIRUS DNA DETECTION KIT	1990-02-01
PMA P880009S002 QIAGEN, INC.	VIRAPAP HUMAN PAPILLOMAVIRUS DNA DETECTION KIT	1989-08-21
PMA P880009S001 QIAGEN, INC.	VIRAPAP HUMAN PAPILLOMAVIRUS DNA DETECTION KIT	1989-06-06
PMA P880009 QIAGEN, INC.	VIRAPAP HUMAN PAPILLOMAVIRUS DNA DETECTION KIT	1988-12-23