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.
Device | VITROS Anti-HBc IgM |
Generic Name | Test, Hepatitis B (b Core, Be Antigen, Be Antibody, B Core Igm) |
Applicant | Ortho-Clinical Diagnostics, Inc.100 Indigo Creek Dr.rochester, NY 14626-5101 PMA NumberP030026 Supplement NumberS037 Date Received09/30/2022 Decision Date01/24/2023 Product Code LOM Advisory Committee Microbiology Supplement Typereal-time Process Supplement Reason Labeling Change - Indications/instructions/shelf Life/tradename Expedited Review Granted? No |
Date Received | 2022-09-30 |
Decision Date | 2023-01-24 |
PMA | P030026 |
Supplement | S037 |
Product Code | LOM |
Advisory Committee | Microbiology |
Supplement Type | Real-time Process |
Supplement Reason | Labeling Change - Indications/instructions/shelf Life/tradename |
Expedited Review | No |
Combination Product | No |
Applicant Address | Ortho-Clinical Diagnostics, Inc. 100 Indigo Creek Dr. rochester, NY 14626-5101 PMA NumberP030026 Supplement NumberS037 Date Received09/30/2022 Decision Date01/24/2023 Product Code LOM Advisory Committee Microbiology Supplement Typereal-time Process Supplement Reason Labeling Change - Indications/instructions/shelf Life/tradename Expedited Review Granted? No Combination ProductNo Approval Order Statement Approval For Revisions To The Package Insert To Include Information On Biotin Interference. |
Supplement Number | Date | Supplement Type |
---|---|---|
P030026 | Original Filing | |
S037 | 2022-09-30 | Real-time Process |
S036 | 2019-05-21 | 30-day Notice |
S035 | 2018-10-16 | Normal 180 Day Track No User Fee |
S034 | 2018-02-21 | Normal 180 Day Track No User Fee |
S033 | 2018-01-16 | 30-day Notice |
S032 | 2018-01-09 | Normal 180 Day Track No User Fee |
S031 | 2015-10-05 | 30-day Notice |
S030 | 2015-08-10 | 30-day Notice |
S029 | 2015-01-16 | 30-day Notice |
S028 | 2013-09-20 | 30-day Notice |
S027 | 2012-11-29 | 30-day Notice |
S026 | 2012-10-17 | 30-day Notice |
S025 | 2012-01-30 | 30-day Notice |
S024 | 2011-10-05 | Real-time Process |
S023 | 2011-05-19 | 30-day Notice |
S022 | 2011-05-16 | 135 Review Track For 30-day Notice |
S021 | 2010-12-08 | 30-day Notice |
S020 | 2010-10-18 | 30-day Notice |
S019 | 2009-12-01 | Normal 180 Day Track No User Fee |
S018 | 2009-05-22 | 30-day Notice |
S017 | 2009-03-06 | 30-day Notice |
S016 | 2009-02-20 | Normal 180 Day Track |
S015 | 2008-11-13 | Normal 180 Day Track No User Fee |
S014 | 2008-02-27 | 30-day Notice |
S013 | 2007-03-08 | 30-day Notice |
S012 | 2007-02-07 | Special (immediate Track) |
S011 | 2006-08-21 | 30-day Notice |
S010 | 2006-05-17 | 30-day Notice |
S009 | 2005-11-14 | 30-day Notice |
S008 | 2005-09-30 | Special (immediate Track) |
S007 | 2005-06-27 | 30-day Notice |
S006 | 2005-06-03 | 30-day Notice |
S005 | 2005-04-07 | 30-day Notice |
S004 | 2004-12-21 | 30-day Notice |
S003 | 2004-12-15 | 30-day Notice |
S002 | 2004-10-26 | 30-day Notice |
S001 | 2004-05-24 | 30-day Notice |
Device ID | PMA | Supp |
---|---|---|
10758750002795 | P030026 | 028 |
10758750001194 | P030026 | 028 |
10758750001187 | P030026 | 028 |