HBSAG IMMULITE ASSAY

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

FDA Premarket Approval P010050 S013

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

Full automation of the filling and packaging line for the immulite chemiluminescent substrate reagent, accessory used with all the immulite assays.

DeviceHBSAG IMMULITE 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 Products, LTD
Date Received2011-08-08
Decision Date2011-09-02
PMAP010050
SupplementS013
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 Products, LTD glyn Rhonwy llanberis, Caernarfon LL55

Supplemental Filings

Supplement NumberDateSupplement Type
P010050Original 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

Device IDPMASupp
00630414971551 P010050 001
00630414971544 P010050 001
00630414971438 P010050 001
00630414947433 P010050 001

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