Approval for a manufacturing site for the cobas e 411 analyzer located at hitachi high-technologies corp. , 1892-1, oazategama, omuta, fukuoka, 836-0004 japan
| Device | Elecsys Anti-HBc II |
| Classification Name | Test, Hepatitis B (b Core, Be Antigen, Be Antibody, B Core Igm) |
| Generic Name | Test, Hepatitis B (b Core, Be Antigen, Be Antibody, B Core Igm) |
| Applicant | ROCHE DIAGNOSTICS CORP. |
| Date Received | 2018-10-26 |
| Decision Date | 2019-04-24 |
| PMA | P100031 |
| Supplement | S026 |
| Product Code | LOM |
| Advisory Committee | Microbiology |
| Supplement Type | Normal 180 Day Track No User Fee |
| Supplement Reason | Location Change - Manufacturer/sterilizer/packager/supplier |
| Expedited Review | No |
| Combination Product | No |
| Applicant Address | ROCHE DIAGNOSTICS CORP. 9115 Hague Rd. indianapolis, IN 46250 |
Supplemental Filings
| Supplement Number | Date | Supplement Type |
|---|
| P100031 | | Original Filing |
| S027 |
2021-09-30 |
Normal 180 Day Track |
| S026 |
2018-10-26 |
Normal 180 Day Track No User Fee |
| S025 |
2018-10-09 |
30-day Notice |
| S024 |
2018-04-17 |
Real-time Process |
| S023 |
2018-03-01 |
Real-time Process |
| S022 | | |
| S021 |
2017-10-11 |
Real-time Process |
| S020 |
2017-09-28 |
Normal 180 Day Track |
| S019 |
2017-08-03 |
30-day Notice |
| S018 |
2017-05-24 |
30-day Notice |
| S017 |
2017-02-21 |
Normal 180 Day Track |
| S016 |
2016-02-16 |
30-day Notice |
| S015 |
2016-01-27 |
30-day Notice |
| S014 |
2016-01-27 |
135 Review Track For 30-day Notice |
| S013 |
2015-10-07 |
30-day Notice |
| S012 |
2014-10-16 |
Real-time Process |
| S011 |
2014-04-04 |
Real-time Process |
| S010 |
2012-11-30 |
30-day Notice |
| S009 |
2012-09-04 |
Normal 180 Day Track |
| S008 |
2012-09-04 |
Normal 180 Day Track |
| S007 | | |
| S006 |
2012-02-29 |
30-day Notice |
| S005 |
2012-01-31 |
135 Review Track For 30-day Notice |
| S004 |
2011-08-29 |
135 Review Track For 30-day Notice |
| S003 |
2011-08-17 |
Normal 180 Day Track No User Fee |
| S002 |
2011-08-17 |
135 Review Track For 30-day Notice |
| S001 |
2011-07-01 |
30-day Notice |
NIH GUDID Devices