This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.
Approval for the change in manufacturing of a critical reagent (taq polymerase)and the conversion of a manual reagent fill process to one that is automated.
| Device | THERASCREEN EGFR RGQ PCR KIT |
| Classification Name | Somatic Gene Mutation Detection System |
| Generic Name | Somatic Gene Mutation Detection System |
| Applicant | QIAGEN MANCHESTER LTD |
| Date Received | 2015-02-18 |
| Decision Date | 2015-08-06 |
| PMA | P120022 |
| Supplement | S010 |
| Product Code | OWD |
| Advisory Committee | Pathology |
| Supplement Type | Normal 180 Day Track |
| Supplement Reason | Change Design/components/specifications/material |
| Expedited Review | No |
| Combination Product | No |
| Applicant Address | QIAGEN MANCHESTER LTD skelton House lloyd Street North manchester M15 6 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P120022 | Original Filing | |
| S022 | 2020-10-23 | Real-time Process |
| S021 | 2020-03-04 | 30-day Notice |
| S020 | 2019-08-28 | Special (immediate Track) |
| S019 | 2018-03-08 | 30-day Notice |
| S018 | 2018-02-16 | Normal 180 Day Track |
| S017 | 2018-01-26 | 30-day Notice |
| S016 | 2017-07-28 | Normal 180 Day Track |
| S015 | 2017-06-29 | 30-day Notice |
| S014 | 2016-12-28 | Normal 180 Day Track |
| S013 | 2016-08-10 | 30-day Notice |
| S012 | 2015-09-28 | Normal 180 Day Track No User Fee |
| S011 | ||
| S010 | 2015-02-18 | Normal 180 Day Track |
| S009 | 2015-01-26 | Real-time Process |
| S008 | 2015-01-26 | Real-time Process |
| S007 | 2015-01-21 | 30-day Notice |
| S006 | 2015-01-21 | 30-day Notice |
| S005 | 2014-12-22 | 30-day Notice |
| S004 | 2014-12-15 | 30-day Notice |
| S003 | ||
| S002 | 2014-11-19 | 30-day Notice |
| S001 | 2014-09-18 | Normal 180 Day Track |