Change to the reagent manufacturing process.
Device | IMMULITE / IMMULITE 1000 HBSAG & IMMULITE 2000 HBSAG |
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 | Siemens Healthcare Diagnostics Products, LTD |
Date Received | 2006-08-04 |
Decision Date | 2006-09-01 |
PMA | P010050 |
Supplement | S005 |
Product Code | LOM |
Advisory Committee | Microbiology |
Supplement Type | 30-day Notice |
Supplement Reason | Process Change - Manufacturer/sterilizer/packager/supplier |
Expedited Review | No |
Combination Product | No |
Applicant Address | Siemens Healthcare Diagnostics Products, LTD glyn Rhonwy llanberis, Caernarfon LL55 |
Supplemental Filings
Supplement Number | Date | Supplement Type |
P010050 | | Original Filing |
S021 |
2022-09-15 |
30-day Notice |
S020 | | |
S019 |
2021-05-12 |
30-day Notice |
S018 |
2020-08-12 |
30-day Notice |
S017 |
2019-11-25 |
30-day Notice |
S016 |
2014-07-02 |
135 Review Track For 30-day Notice |
S015 |
2011-12-19 |
135 Review Track For 30-day Notice |
S014 |
2011-08-16 |
30-day Notice |
S013 |
2011-08-08 |
30-day Notice |
S012 |
2011-02-18 |
Real-time Process |
S011 |
2010-09-29 |
Normal 180 Day Track |
S010 |
2009-11-02 |
Normal 180 Day Track No User Fee |
S009 | | |
S008 |
2009-05-13 |
Real-time Process |
S007 |
2008-12-02 |
Normal 180 Day Track |
S006 |
2008-11-10 |
Normal 180 Day Track No User Fee |
S005 |
2006-08-04 |
30-day Notice |
S004 | | |
S003 |
2003-05-22 |
30-day Notice |
S002 | | |
S001 |
2002-11-20 |
Real-time Process |
NIH GUDID Devices