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 changing bsa raw material.
Device | ETI-COREK-IGMK PLUS KIT |
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 | DIASORIN, INC. |
Date Received | 2009-11-13 |
Decision Date | 2010-05-21 |
PMA | P990044 |
Supplement | S010 |
Product Code | LOM |
Advisory Committee | Microbiology |
Supplement Type | 135 Review Track For 30-day Notice |
Supplement Reason | Process Change - Manufacturer/sterilizer/packager/supplier |
Expedited Review | No |
Combination Product | No |
Applicant Address | DIASORIN, INC. 1951 Northwestern Ave. stillwater, MN 55082-0285 |
Supplement Number | Date | Supplement Type |
---|---|---|
P990044 | Original Filing | |
S029 | 2021-11-23 | 30-day Notice |
S028 | 2020-07-16 | 30-day Notice |
S027 | 2019-08-28 | 30-day Notice |
S026 | 2019-06-18 | 30-day Notice |
S025 | 2018-05-30 | 30-day Notice |
S024 | 2018-03-30 | 30-day Notice |
S023 | ||
S022 | 2018-02-14 | 30-day Notice |
S021 | 2017-09-18 | 30-day Notice |
S020 | 2017-04-25 | 30-day Notice |
S019 | 2017-03-29 | 30-day Notice |
S018 | 2016-05-10 | 30-day Notice |
S017 | 2014-06-05 | 30-day Notice |
S016 | 2013-12-27 | 30-day Notice |
S015 | 2013-06-05 | 30-day Notice |
S014 | 2012-11-09 | Special (immediate Track) |
S013 | ||
S012 | 2012-02-17 | 30-day Notice |
S011 | 2011-10-18 | 30-day Notice |
S010 | 2009-11-13 | 135 Review Track For 30-day Notice |
S009 | 2009-11-13 | Real-time Process |
S008 | 2006-12-29 | 30-day Notice |
S007 | 2005-06-03 | 30-day Notice |
S006 | ||
S005 | 2004-04-05 | 30-day Notice |
S004 | 2003-04-14 | 30-day Notice |
S003 | 2003-04-09 | Normal 180 Day Track No User Fee |
S002 | 2002-10-17 | 30-day Notice |
S001 | 2002-01-07 | Normal 180 Day Track |