VITROS IMMUNODIAGNOSTIC PRODUCTS HBEAG REAGENT PACK AND CALIBRATOR

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

FDA Premarket Approval P090028 S007

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

Change to the manufacturing process for streptavidin coated (sac) wells included in the vitros immunodiagnostic products hbeag reagent pack and calibrator.

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 Received2013-09-20
Decision Date2013-10-17
PMAP090028
SupplementS007
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
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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