Duplication for manufacture of reagent components at an approved manufacturing site.
Device | Aptima HPV Assay |
Classification Name | Kit, Rna Detection, Human Papillomavirus |
Generic Name | Kit, Rna Detection, Human Papillomavirus |
Applicant | GEN-PROBE INCORPORATED |
Date Received | 2018-03-15 |
Decision Date | 2018-04-13 |
PMA | P100042 |
Supplement | S017 |
Product Code | OYB |
Advisory Committee | Microbiology |
Supplement Type | 30-day Notice |
Supplement Reason | Process Change - Manufacturer/sterilizer/packager/supplier |
Expedited Review | No |
Combination Product | No |
Applicant Address | GEN-PROBE INCORPORATED 10210 Genetic Center Drive san Diego, CA 92121 |
Supplemental Filings
Supplement Number | Date | Supplement Type |
P100042 | | Original Filing |
S033 |
2022-01-19 |
30-day Notice |
S032 | | |
S031 |
2020-07-09 |
30-day Notice |
S030 |
2020-05-14 |
30-day Notice |
S029 |
2020-02-03 |
30-day Notice |
S028 |
2019-12-23 |
Real-time Process |
S027 | | |
S026 |
2019-08-21 |
30-day Notice |
S025 |
2019-08-02 |
30-day Notice |
S024 | | |
S023 |
2019-03-27 |
30-day Notice |
S022 |
2019-03-18 |
Real-time Process |
S021 |
2019-02-21 |
30-day Notice |
S020 |
2018-12-31 |
Real-time Process |
S019 |
2018-08-31 |
30-day Notice |
S018 |
2018-08-16 |
30-day Notice |
S017 |
2018-03-15 |
30-day Notice |
S016 |
2018-02-08 |
30-day Notice |
S015 |
2017-12-20 |
30-day Notice |
S014 |
2017-10-10 |
30-day Notice |
S013 |
2017-09-01 |
Normal 180 Day Track |
S012 |
2017-03-17 |
Real-time Process |
S011 |
2016-08-15 |
30-day Notice |
S010 |
2016-04-25 |
30-day Notice |
S009 |
2015-10-16 |
30-day Notice |
S008 |
2015-08-28 |
135 Review Track For 30-day Notice |
S007 |
2015-08-12 |
Normal 180 Day Track |
S006 | | |
S005 |
2015-03-04 |
30-day Notice |
S004 |
2014-12-24 |
Normal 180 Day Track No User Fee |
S003 |
2014-06-09 |
30-day Notice |
S002 |
2014-04-17 |
Real-time Process |
S001 |
2012-10-04 |
Normal 180 Day Track |
NIH GUDID Devices