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 implementation of system software 06-04 on the cobas e 602 to address a software limitation
Device | Elecsys Anti-HBc IgM |
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 | 2017-10-11 |
Decision Date | 2017-12-20 |
PMA | P110031 |
Supplement | S020 |
Product Code | LOM |
Advisory Committee | Microbiology |
Supplement Type | Real-time Process |
Supplement Reason | Change Design/components/specifications/material |
Expedited Review | No |
Combination Product | No |
Applicant Address | ROCHE DIAGNOSTICS CORP. 9115 Hague Road p.o. Box 50416 indianapolis, IN 46250-0457 |
Supplement Number | Date | Supplement Type |
---|---|---|
P110031 | Original Filing | |
S024 | 2018-10-26 | Normal 180 Day Track No User Fee |
S023 | 2018-10-09 | 30-day Notice |
S022 | 2018-03-01 | Real-time Process |
S021 | ||
S020 | 2017-10-11 | Real-time Process |
S019 | 2017-08-03 | 30-day Notice |
S018 | 2017-05-24 | 30-day Notice |
S017 | 2016-12-07 | Real-time Process |
S016 | 2016-09-07 | Normal 180 Day Track No User Fee |
S015 | 2016-07-11 | 135 Review Track For 30-day Notice |
S014 | 2016-02-16 | 30-day Notice |
S013 | 2016-01-27 | 30-day Notice |
S012 | 2016-01-27 | 135 Review Track For 30-day Notice |
S011 | 2015-10-07 | 30-day Notice |
S010 | 2013-07-19 | Special (immediate Track) |
S009 | ||
S008 | 2012-11-30 | 30-day Notice |
S007 | ||
S006 | 2012-02-29 | 30-day Notice |
S005 | 2012-02-02 | 30-day Notice |
S004 | 2012-02-02 | 30-day Notice |
S003 | 2012-02-02 | 30-day Notice |
S002 | 2012-01-31 | 135 Review Track For 30-day Notice |
S001 | 2012-01-31 | Normal 180 Day Track No User Fee |