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Qiagen, Inc.

15 FDA 510(k) clearances · PMA applicant

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RecordFirmDate
PartoSure Test (P160052/S001)Qiagen, Inc.2019-10-11
artus CMV RGQ MDx Kit and artus CMV QS-RGO MDx Kit (P130027/S006)Qiagen, Inc.2018-09-26
PartoSure test (P160052)Qiagen, Inc.2018-04-11
artus CMV RGQ MDx Kit and artus CMV QS_RGQ MDx Kit (P130027/S005)Qiagen, Inc.2018-04-06
artus CMV RGQ MDx Kit and artus CMV QS-RGQ MDx Kit (P130027/S004)Qiagen, Inc.2018-03-13
Artus CMV RGQ and QS-RGQ MDx Kit (P130027/S003)Qiagen, Inc.2017-11-15
ARTUS CMV RGQ MDX KIT (P130027/S002)Qiagen, Inc.2017-06-02
ARTUS CMV RGQ MDX KIT (P130027/S001)Qiagen, Inc.2015-07-09
ARTUS CMV RGQ MDX KIT (P130027)Qiagen, Inc.2014-06-02
VIRAPAP HUMAN PAPILLOMAVIRUS DNA DETECTION KIT (P880009/S005)Qiagen, Inc.1993-05-17
VIRAPAP HUMAN PAPILLOMAVIRUS DNA DETECTION KIT (P880009/S004)Qiagen, Inc.1991-08-19
VIRAPAP HUMAN PAPILLOMAVIRUS DNA DETECTION KIT (P880009/S003)Qiagen, Inc.1990-02-01
VIRAPAP HUMAN PAPILLOMAVIRUS DNA DETECTION KIT (P880009/S002)Qiagen, Inc.1989-08-21
VIRAPAP HUMAN PAPILLOMAVIRUS DNA DETECTION KIT (P880009/S001)Qiagen, Inc.1989-06-06
VIRAPAP HUMAN PAPILLOMAVIRUS DNA DETECTION KIT (P880009)Qiagen, Inc.1988-12-23

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Every clearance here is in the API, with alerts when new ones post.