IMMULITE/IMMULITE 1000 AND IMMULITE 2000 ANTI-HBC

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

FDA Premarket Approval P010051 S003

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

Approval for changes in the manufacturing process which add an incoming raw material test.

DeviceIMMULITE/IMMULITE 1000 AND IMMULITE 2000 ANTI-HBC
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 Received2005-08-17
Decision Date2005-11-02
PMAP010051
SupplementS003
Product CodeLOM
Advisory CommitteeMicrobiology
Supplement TypeSpecial (immediate Track)
Expedited ReviewNo
Combination Product No
Applicant Address Siemens Healthcare Diagnostics Products, LTD glyn Rhonwy llanberis, Caernarfon LL55

Supplemental Filings

Supplement NumberDateSupplement Type
P010051Original Filing
S017 2022-09-15 30-day Notice
S016
S015 2022-02-28 30-day Notice
S014 2020-12-22 Real-time Process
S013 2020-08-12 30-day Notice
S012 2019-11-25 30-day Notice
S011 2011-12-19 135 Review Track For 30-day Notice
S010 2011-08-16 30-day Notice
S009 2011-08-08 30-day Notice
S008 2011-02-18 Real-time Process
S007 2009-11-02 Normal 180 Day Track No User Fee
S006
S005 2008-11-10 Normal 180 Day Track No User Fee
S004 2005-12-22 Real-time Process
S003 2005-08-17 Special (immediate Track)
S002
S001 2002-11-20 Real-time Process

NIH GUDID Devices

Device IDPMASupp
00630414970981 P010051 001
00630414970974 P010051 001

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.