FDA PMA FDA Class 2 Approved (Reclassification) 🇺🇸 United States

Assay, Enzyme Linked Immunosorbent, Hepatitis C Virus

PMA: P140021 · Decision Jun 11, 2015
Classifications
1
FEI Numbers
24
Registration Numbers
24

Basic Information

Device Name
Assay, Enzyme Linked Immunosorbent, Hepatitis C Virus
Trade Name
ELECSYS ANTI-HCV II IMMUNOASSAY, ELECSYS PRECICONTROL ANTI-HCV
PMA Number
P140021
Device Class
FDA Class 2
Product Code
MZO
Generic Name
Assay, enzyme linked immunosorbent, hepatitis c virus
Medical Specialty
Unknown
Advisory Committee
Microbiology
Decision
Approved (Reclassification)
Decision Code
APRL
Decision Date
June 11, 2015
Date Received
October 1, 2014
Expedited Review
N
Docket Number
15M-2217

Advisory Committee Statement

APPROVAL FOR THE ELECSYS ANTI-HCV II IMMUNOASSAY AND ELECSYS PRECICONTROL ANTI-HCV. THIS DEVICE IS INDICATED FOR: ELECSYS ANTI-HCV II IMMUNOASSAYIMMUNOASSAY FOR THE IN VITRO QUALITATIVE DETECTION OF ANTIBODIES TO HEPATITIS C VIRUS (HCV) IN HUMAN ADULT AND PEDIATRIC (AGES 18 MONTHS THROUGH 21 YEARS) SERUM AND PLASMA (POTASSIUM EDTA, LITHIUM HEPARIN, SODIUM HEPARIN, AND SODIUM CITRATE). ASSAY RESULTS, IN CONJUNCTION WITH OTHER LABORATORY RESULTS AND CLINICAL INFORMATION, MAY BE USED TO AID IN THE PRESUMPTIVE DIAGNOSIS OF HCV INFECTION IN PERSONS WITH SIGNS AND SYMPTOMS OF HEPATITIS AND IN PERSONS AT RISK FOR HEPATITIS C INFECTION. THE TEST DOES NOT DETERMINE THE STATE OF INFECTION OR ASSOCIATED DISEASE.THE ELECTROLUMINESCENCE IMMUNOASSAY ECLIA IS INTENDED FOR USE ON THE ROCHE COBAS E 601 IMMUNOASSAY ANALYZER.ELECSYS PRECICONTROL ANTI-HCV ELECSYS PRECICONTROL ANTI-HCV IS USED FOR QUALITY CONTROL OF THE ELECSYS ANTI-HCV IMMUNOASSAY ON THE COBAS E 601 AND COBAS E 602 IMMUNOASSAY ANALYZERS AND THE ELECSYS ANTI-HCV II IMMUNOASSAY ON THE COBAS E 601 IMMUNOASSAY ANALYZER.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MZO Assay, Enzyme Linked Immunosorbent, Hepatitis C Virus