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ORAQUICK HCV RAPID ANTIBODY TEST

FDA premarket approval P080027/S001 · decided 2011-02-18

Approval details

PMA number
P080027
Supplement
S001
Supplement type
Panel Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
ORAQUICK HCV RAPID ANTIBODY TEST
Generic name
Assay, enzyme linked immunosorbent, hepatitis c virus
Applicant
OraSure Technologies, Inc.
Date received
2010-08-03
Decision date
2011-02-18
Days to decision
199 days
Decision code
APPR
Product code
MZO
Advisory committee
Microbiology
Expedited review
No
Location
Bethlehem, PA
Statement
APPROVAL FOR THE ORAQUICK HCV RAPID ANTIBODY TEST IS A SINGLE-USE IMMUNOASSAY FOR THE QUALITATIVE DETECTION OF ANTIBODIES TO HEPATITIS C VIRUS (ANTI-HCV) IN FINGERSTICK WHOLE BLOOD SPECIMENS AND VENIPUNCTURE WHOLE BLOOD SPECIMENS (EDTA, SODIUM HEPARIN, LITHIUM HEPARIN, AND SODIUM CITRATE) FROM INDIVIDUALS 15 YEARS OR OLDER. THE ORAQUICK HCV RAPID ANTIBODY TEST RESULTS, IN CONJUNCTION WITH OTHER LABORATORY RESULTS AND CLINICAL INFORMATION, MAY BE USED TO PROVIDE PRESUMPTIVE EVIDENCE OF INFECTION

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510(k) clearances by this applicant

RecordFirmDate
OraQuick Ebola Rapid Antigen Test (DEN190025)OraSure Technologies, Inc.2019-10-10
COMPOUND W FREEZE OFF WART REMOVAL SYSTEM (K060859)OraSure Technologies, Inc.2006-07-18
HISTOFREEZER WART REMOVAL SYSTEM OR OTHER PROPRIETARY NAME (K023487)OraSure Technologies, Inc.2003-03-20
OTI BENZODIAZEPINES INTERCEPT MICRO-PLATE EIA MODEL #1110I (K013882)OraSure Technologies, Inc.2002-04-17
UPLINK TEST SYSTEM (K020371)OraSure Technologies, Inc.2002-04-03
INTERCEPT ORAL FLUID DRUG TEST ORAL SPECIMEN COLLECTION DEVICE, MODEL 503-XXXX (K011057)OraSure Technologies, Inc.2001-06-06
STC CANNABINOIDS INTERCEPT MICRO-PLATE EIA, MODEL 1118I (K002375)OraSure Technologies, Inc.2001-01-26
STC BARBITURATES INTERCEPT MICRO-PLATE EIA, MODEL 1108I (K001976)OraSure Technologies, Inc.2000-12-06