This medical device has supplements. The device description/function or indication may have changed. Be sure to look at the supplements to get an up-to-date information on device changes. The labeling included below is the version at time of approval of the original pma or panel track supplement and may not represent the most recent labeling.
| Device | VIRAPAP HUMAN PAPILLOMAVIRUS DNA DETECTION KIT |
| Classification Name | Kit, Dna Detection, Human Papillomavirus |
| Generic Name | Kit, Dna Detection, Human Papillomavirus |
| Applicant | QIAGEN, INC. |
| Date Received | 1988-02-17 |
| Decision Date | 1988-12-23 |
| Notice Date | 1989-02-28 |
| PMA | P880009 |
| Supplement | S |
| Product Code | MAQ |
| Docket Number | 88M-0446 |
| Advisory Committee | Microbiology |
| Expedited Review | No |
| Combination Product | No |
| Applicant Address | QIAGEN, INC. 1201 Clopper Road gaithersburg, MD 20878 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P880009 | Original Filing | |
| S005 | 1991-10-18 | Normal 180 Day Track |
| S004 | 1991-05-24 | Normal 180 Day Track |
| S003 | 1989-09-18 | Normal 180 Day Track |
| S002 | 1989-06-16 | Normal 180 Day Track |
| S001 | 1989-04-04 | Normal 180 Day Track |