Athena Multi-Lyte Ebv Vca Igm Test System

FDA 510(k) K042092 · Zeus Scientific, Inc.

Substantially Equivalent

510(k) numberK042092

Submission

Device name
Athena Multi-Lyte Ebv Vca Igm Test System
Applicant
Zeus Scientific, Inc.
Raritan, NJ, US
Received
August 3, 2004
Decision date
April 12, 2005
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
LJN – Antibody Igm, If, Epstein-Barr Virus
Device class
Class I (low risk)
Regulation
21 CFR 866.3235
Specialty
Microbiology

Other 510(k)s with product code LJN

510(k)DeviceApplicantDecision
K123021Bioplex 2200 Ebv Igm KitLJN · Traditional Bio-Rad Laboratories11/02/2012SE
K073381Plexus Ebv Igm Multi-Analyte Diagnostics, Model: MP0600MLJN · Traditional Focus Diagnostics, Inc.08/04/2008SE
K033780Modification to Seraquest Vca IgmLJN · Special Quest Intl., Inc.01/15/2004SE
K990977Seraquest Eb Vac IgmLJN · Traditional Quest Intl., Inc.10/06/1999SE
K991459Copalis Ebv-M Antibody AssayLJN · Traditional DiaSorin, Inc.05/14/1999SE
K973939Immunowell Vca Igm TestLJN · Traditional Genbio08/10/1998SE
K931520Epstein-Barr Virus Vca (Igm) Recomb Immun AntibodyLJN · Traditional Mrl Diagnostics04/26/1994SE
K930020Ortho*Epstein-Barr Virus Vca-Igm Antibody ElisaLJN · Traditional Ortho Diagnostic Systems, Inc.07/16/1993SE
K922331Bartels Epstein-Barr Virus Igm EiaLJN · Traditional Baxter Diagnostics, Inc.09/02/1992SE
K915348Ebv-Vca Igm ElisaLJN · Traditional Pharmacia Diagnostics, Inc.02/14/1992SE

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Questions and answers

When was Athena Multi-Lyte Ebv Vca Igm Test System cleared by the FDA?

Athena Multi-Lyte Ebv Vca Igm Test System (K042092) received a 510(k) decision of Substantially Equivalent on April 12, 2005, 252 days after the submission was received.

What is the product code of K042092?

The FDA product code is LJN – Antibody Igm, If, Epstein-Barr Virus, a Class I (low risk) device regulated under 21 CFR 866.3235.