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 a manufacturing site located at abbott ireland diagnostics division in sligo, ireland.
Device | AXSYM CORE 2.0 |
Generic Name | Test, Hepatitis B (b Core, Be Antigen, Be Antibody, B Core Igm) |
Applicant | ABBOTT LABORATORIES INC |
Date Received | 2011-01-31 |
Decision Date | 2011-04-15 |
PMA | P060012 |
Supplement | S006 |
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 | ABBOTT LABORATORIES INC 100 Abbott Park Road ap5n-2, Dept. 09vb abbott Park, IL 60064 |
Supplement Number | Date | Supplement Type |
---|---|---|
P060012 | Original Filing | |
S010 | 2012-11-13 | 30-day Notice |
S009 | 2011-11-02 | 135 Review Track For 30-day Notice |
S008 | 2011-09-07 | Special (immediate Track) |
S007 | 2011-03-21 | 135 Review Track For 30-day Notice |
S006 | 2011-01-31 | Normal 180 Day Track No User Fee |
S005 | 2010-11-01 | Normal 180 Day Track No User Fee |
S004 | 2010-09-27 | 30-day Notice |
S003 | 2010-09-21 | 30-day Notice |
S002 | 2010-05-19 | 30-day Notice |
S001 | 2007-01-17 | 30-day Notice |