VITROS Immunodiagnostic Products HBeAg Reagent Pack and Calibrator

FDA Premarket Approval P090028 S018

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

DeviceVITROS Immunodiagnostic Products HBeAg Reagent Pack and Calibrator
Generic NameTest, Hepatitis B (b Core, Be Antigen, Be Antibody, B Core Igm)
ApplicantOrtho-Clinical Diagnostics, Inc.100 Indigo Creek Dr.rochester, NY 14626-5101 PMA NumberP090028 Supplement NumberS018 Date Received09/30/2022 Decision Date01/24/2023 Product Code LOM  Advisory Committee Microbiology Supplement Typereal-time Process Supplement Reason Labeling Change - Indications/instructions/shelf Life/tradename Expedited Review Granted? No
Date Received2022-09-30
Decision Date2023-01-24
PMAP090028
SupplementS018
Product CodeLOM 
Advisory CommitteeMicrobiology
Supplement TypeReal-time Process
Supplement ReasonLabeling Change - Indications/instructions/shelf Life/tradename
Expedited ReviewNo
Combination ProductNo
Applicant AddressOrtho-Clinical Diagnostics, Inc.
100 Indigo Creek Dr.
rochester, NY 14626-5101 PMA NumberP090028 Supplement NumberS018 Date Received09/30/2022 Decision Date01/24/2023 Product Code LOM  Advisory Committee Microbiology Supplement Typereal-time Process Supplement Reason Labeling Change - Indications/instructions/shelf Life/tradename Expedited Review Granted? No Combination ProductNo Approval Order Statement  
Approval For Revisions To The Package Insert To Include Information On Biotin Interference.

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

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