ADVIA CENTAUR HBC TOTAL ASSAY

Test, Hepatitis B (b Core, Be Antigen, Be Antibody, B Core Igm)

FDA Premarket Approval P040004 S008

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.

Pre-market Approval Supplement Details

Adding an in-process step to the preparation of the labeled antigen.

DeviceADVIA CENTAUR HBC TOTAL ASSAY
Classification NameTest, Hepatitis B (b Core, Be Antigen, Be Antibody, B Core Igm)
Generic NameTest, Hepatitis B (b Core, Be Antigen, Be Antibody, B Core Igm)
ApplicantSIEMENS HEALTHCARE DIAGNOSTICS
Date Received2012-01-09
Decision Date2012-02-03
PMAP040004
SupplementS008
Product CodeLOM
Advisory CommitteeMicrobiology
Supplement Type30-day Notice
Supplement ReasonProcess Change - Manufacturer/sterilizer/packager/supplier
Expedited ReviewNo
Combination Product No
Applicant Address SIEMENS HEALTHCARE DIAGNOSTICS 333 Coney Street walpole, MA 02032-1516

Supplemental Filings

Supplement NumberDateSupplement Type
P040004Original Filing
S021 2022-03-22 30-day Notice
S020 2021-04-01 30-day Notice
S019 2020-12-22 Real-time Process
S018 2020-07-31 30-day Notice
S017 2020-03-09 30-day Notice
S016 2020-02-21 30-day Notice
S015 2019-02-01 30-day Notice
S014 2018-07-19 Real-time Process
S013 2017-07-17 Normal 180 Day Track
S012 2015-07-13 Normal 180 Day Track
S011 2015-06-11 30-day Notice
S010 2014-09-09 Normal 180 Day Track
S009 2012-03-26 Normal 180 Day Track No User Fee
S008 2012-01-09 30-day Notice
S007 2010-01-08 30-day Notice
S006 2009-05-18 Normal 180 Day Track
S005 2009-03-31 Normal 180 Day Track
S004 2009-03-09 Normal 180 Day Track No User Fee
S003 2009-02-04 30-day Notice
S002 2008-08-26 Normal 180 Day Track
S001

NIH GUDID Devices

Device IDPMASupp
00630414498089 P040004 000
00630414599212 P040004 002
00630414599205 P040004 002
00630414498096 P040004 002
00630414301303 P040004 002

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