IMMULITE® 2000 HBsAg and IMMULITE® 2000 HBsAg Confirmatory Kit’

FDA Premarket Approval P010050 S021

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

DeviceIMMULITE® 2000 HBsAg and IMMULITE® 2000 HBsAg Confirmatory Kit’
Generic NameTest, Hepatitis B (b Core, Be Antigen, Be Antibody, B Core Igm)
ApplicantSiemens Healthcare Diagnostics Products, LTDglyn Rhonwyllanberis, Caernarfon LL55 PMA NumberP010050 Supplement NumberS021 Date Received09/15/2022 Decision Date10/14/2022 Product Code LOM  Advisory Committee Microbiology Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
Date Received2022-09-15
Decision Date2022-10-14
PMAP010050
SupplementS021
Product CodeLOM 
Advisory CommitteeMicrobiology
Supplement Type30-day Notice
Supplement ReasonProcess Change - Manufacturer/sterilizer/packager/supplier
Expedited ReviewNo
Combination ProductNo
Applicant AddressSiemens Healthcare Diagnostics Products, LTD
glyn Rhonwy
llanberis, Caernarfon LL55 PMA NumberP010050 Supplement NumberS021 Date Received09/15/2022 Decision Date10/14/2022 Product Code LOM  Advisory Committee Microbiology Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No Combination ProductNo Approval Order Statement  
Change In Material Composition Of The Glass Bulb Used In PMT (Photo Multiplier Tube) Assembly On The IMMULITE Family Of Instruments.

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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