VITROS IMMUNODIAGNOSTIC PRODUCTS HBSAG REAGENT PACK AND CALIBRATOR

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

FDA Premarket Approval P000044 S029

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

Changing the timing of the tests in the qa release test from sequential to concurrent, described as the single test.

DeviceVITROS IMMUNODIAGNOSTIC PRODUCTS HBSAG REAGENT PACK AND CALIBRATOR
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)
ApplicantOrtho-Clinical Diagnostics, Inc.
Date Received2012-01-30
Decision Date2012-02-23
PMAP000044
SupplementS029
Product CodeLOM
Advisory CommitteeMicrobiology
Supplement Type30-day Notice
Supplement ReasonProcess Change - Manufacturer/sterilizer/packager/supplier
Expedited ReviewNo
Combination Product No
Applicant Address Ortho-Clinical Diagnostics, Inc. 100 Indigo Creek Dr. rochester, NY 14626-5101

Supplemental Filings

Supplement NumberDateSupplement Type
P000044Original Filing
S040 2019-05-21 30-day Notice
S039 2018-10-16 Normal 180 Day Track No User Fee
S038 2018-02-21 Normal 180 Day Track No User Fee
S037 2018-01-09 Normal 180 Day Track No User Fee
S036 2017-10-17 30-day Notice
S035 2017-05-30 30-day Notice
S034 2016-03-02 30-day Notice
S033 2015-10-29 30-day Notice
S032 2015-08-10 30-day Notice
S031 2015-06-25 30-day Notice
S030 2012-10-17 30-day Notice
S029 2012-01-30 30-day Notice
S028 2011-10-05 Real-time Process
S027 2011-08-19 30-day Notice
S026 2011-04-28 30-day Notice
S025 2010-10-18 30-day Notice
S024 2010-08-06 30-day Notice
S023 2009-12-01 Normal 180 Day Track No User Fee
S022 2009-09-30 30-day Notice
S021 2009-03-06 30-day Notice
S020 2009-02-02 Normal 180 Day Track
S019 2008-11-13 Normal 180 Day Track No User Fee
S018 2008-05-15 30-day Notice
S017 2008-01-23 30-day Notice
S016 2007-03-21 30-day Notice
S015 2007-03-12 30-day Notice
S014 2006-08-08 30-day Notice
S013 2006-05-25 Real-time Process
S012 2006-05-12 30-day Notice
S011 2006-03-15 30-day Notice
S010 2005-11-18 30-day Notice
S009 2005-10-26 30-day Notice
S008 2005-09-02 30-day Notice
S007 2005-07-13 30-day Notice
S006 2005-04-08 Special (immediate Track)
S005 2004-11-15 30-day Notice
S004 2004-10-26 30-day Notice
S003 2003-03-06 30-day Notice
S002 2001-05-29 30-day Notice
S001 2001-05-04 30-day Notice

NIH GUDID Devices

Device IDPMASupp
10758750002764 P000044 030
10758750001088 P000044 030
10758750001071 P000044 030
10758750001064 P000044 030

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