VITROS IMMUNODIAGNOSTIC PRODUCTS HBEAG REAGENT PACK AND CALIBRATOR

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

FDA Premarket Approval P090028 S004

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

Modifications to the component parts of the luminometer signal processor board (lspb). The lspb is used on the vitros eci/eciq immunodiagnostic system, the vitros 3600 immunodiagnostic system and the vitros 5600 integrated system.

DeviceVITROS IMMUNODIAGNOSTIC PRODUCTS HBEAG 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 Received2012-10-17
Decision Date2012-11-13
PMAP090028
SupplementS004
Product CodeLOM
Advisory CommitteeMicrobiology
Supplement Type30-day Notice
Expedited ReviewNo
Combination Product No
Applicant Address Ortho-Clinical Diagnostics, Inc. 100 Indigo Creek Dr. rochester, NY 14626-5101

Supplemental Filings

Supplement NumberDateSupplement Type
P090028Original Filing
S018 2022-09-30 Real-time Process
S017 2019-05-21 30-day Notice
S016 2018-10-16 Normal 180 Day Track No User Fee
S015 2018-02-21 Normal 180 Day Track No User Fee
S014 2018-02-12 30-day Notice
S013 2018-01-09 Normal 180 Day Track No User Fee
S012
S011 2017-09-25 30-day Notice
S010 2016-12-02 Normal 180 Day Track
S009 2015-08-10 30-day Notice
S008 2015-06-25 30-day Notice
S007 2013-09-20 30-day Notice
S006 2012-11-29 30-day Notice
S005 2012-11-15 30-day Notice
S004 2012-10-17 30-day Notice
S003 2012-09-19 30-day Notice
S002 2012-03-22 30-day Notice
S001 2011-10-11 30-day Notice

NIH GUDID Devices

Device IDPMASupp
10758750001453 P090028 007
10758750001446 P090028 007

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