IMMULITE 2000 Anti-HBc

FDA Premarket Approval P010051 S012

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

To modify the resin used in manufacture of reaction tubes

DeviceIMMULITE 2000 Anti-HBc
Generic NameTest, Hepatitis B (b Core, Be Antigen, Be Antibody, B Core Igm)
ApplicantSiemens Healthcare Diagnostics Products, LTD
Date Received2019-11-25
Decision Date2019-12-19
PMAP010051
SupplementS012
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
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.