VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HCV REAGENT PACK AND CALIBRATOR

Assay, Enzyme Linked Immunosorbent, Hepatitis C Virus

FDA Premarket Approval P010021 S003

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 in the manufacturing equipment and manufacturing process steps acceptance criteria associated with this equipment change. The proposed changes affect the manufacturing of vitros immunodiagnostic products anti-hcv reagent pack.

DeviceVITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HCV REAGENT PACK AND CALIBRATOR
Classification NameAssay, Enzyme Linked Immunosorbent, Hepatitis C Virus
Generic NameAssay, Enzyme Linked Immunosorbent, Hepatitis C Virus
ApplicantOrtho-Clinical Diagnostics, Inc.
Date Received2004-07-16
Decision Date2004-07-30
PMAP010021
SupplementS003
Product CodeMZO
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
P010021Original Filing
S033 2020-07-20 30-day Notice
S032 2019-05-21 30-day Notice
S031 2018-10-16 Normal 180 Day Track No User Fee
S030 2018-02-21 Normal 180 Day Track No User Fee
S029 2018-01-09 Normal 180 Day Track No User Fee
S028 2016-10-21 30-day Notice
S027 2015-08-10 30-day Notice
S026 2015-06-25 30-day Notice
S025 2014-11-17 135 Review Track For 30-day Notice
S024 2013-02-08 30-day Notice
S023 2012-10-17 30-day Notice
S022 2012-01-30 30-day Notice
S021 2011-10-05 Real-time Process
S020 2011-06-14 135 Review Track For 30-day Notice
S019 2011-03-24 135 Review Track For 30-day Notice
S018 2010-04-26 30-day Notice
S017 2009-12-01 Normal 180 Day Track No User Fee
S016 2009-03-30 Normal 180 Day Track
S015 2009-03-06 30-day Notice
S014 2008-11-13 Normal 180 Day Track No User Fee
S013 2008-03-20 Real-time Process
S012 2008-01-23 30-day Notice
S011 2007-06-05 30-day Notice
S010 2007-03-28 30-day Notice
S009
S008 2005-11-16 30-day Notice
S007 2005-09-16 Normal 180 Day Track
S006 2005-06-27 135 Review Track For 30-day Notice
S005 2005-02-02 Special (immediate Track)
S004 2004-10-26 30-day Notice
S003 2004-07-16 30-day Notice
S002 2004-07-07 30-day Notice
S001 2003-04-11 30-day Notice

NIH GUDID Devices

Device IDPMASupp
10758750002801 P010021 024
10758750001101 P010021 024
10758750001095 P010021 024

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