Note: 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. |
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Device | LIAISON® XL MUREX Anti-HBe and LIAISON® XL MUREX Control Anti-HBe |
Generic Name | Test, hepatitis b (b core, be antigen, be antibody, b core igm) |
Applicant | DiaSorin Inc. 1951 Northwestern Avenue Stillwater, MN 55082 |
PMA Number | P180049 |
Supplement Number | S013 |
Date Received | 08/31/2023 |
Decision Date | 09/28/2023 |
Product Code |
LOM |
Advisory Committee |
Microbiology |
Supplement Type | 30-Day Notice |
Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement Transfer of logistics activities for the storage warehouse. |
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