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.
Manufacturing process changes
Device | LIAISON XL Murex Anti-HBc and LIAISON XL Murex Control Anti-HBc |
Generic Name | Test, Hepatitis B (b Core, Be Antigen, Be Antibody, B Core Igm) |
Applicant | DiaSorin Inc. |
Date Received | 2020-07-16 |
Decision Date | 2020-08-13 |
PMA | P180038 |
Supplement | S003 |
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 | DiaSorin Inc. 1951 Northwestern Avenue stillwater, MN 55082 |
Supplement Number | Date | Supplement Type |
---|---|---|
P180038 | Original Filing | |
S014 | 2022-11-10 | 30-day Notice |
S013 | ||
S012 | 2022-04-05 | Real-time Process |
S011 | 2022-04-05 | 30-day Notice |
S010 | 2022-02-04 | Real-time Process |
S009 | 2021-11-23 | 30-day Notice |
S008 | 2021-11-23 | 30-day Notice |
S007 | 2021-11-23 | 30-day Notice |
S006 | ||
S005 | 2021-05-27 | Real-time Process |
S004 | ||
S003 | 2020-07-16 | 30-day Notice |
S002 | 2020-06-18 | Real-time Process |
S001 | 2020-02-13 | Real-time Process |