Is Ebv-Ea-D Igg Elisa Test System

FDA 510(k) K981831 · Diamedix Corp.

Substantially Equivalent

510(k) numberK981831

Submission

Device name
Is Ebv-Ea-D Igg Elisa Test System
Applicant
Diamedix Corp.
Columbia, MD, US
Received
May 22, 1998
Decision date
February 16, 1999
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GNP – Antiserum, Cf, Epstein-Barr Virus
Device class
Class I (low risk)
Regulation
21 CFR 866.3235
Specialty
Microbiology

Other 510(k)s with product code GNP

510(k)DeviceApplicantDecision
K020717Ebv V Vca Igm Elisa Kit Model# EBM-200GNP · Traditional Pan Bio Pty. , Ltd.06/13/2002SE
K020707Ebv-Ebna Igg Elisa Kit, Model EBG-100GNP · Traditional Pan Bio Pty. , Ltd.06/13/2002SE
K020706Ebv-Vca Igg Elisa Test, Model EBG-100GNP · Traditional Pan Bio Pty. , Ltd.06/13/2002SE
K981829Is EBV-EBNA-1 Igg Elisa Test SystemGNP · Traditional Diamedix Corp.02/16/1999SE
K901156Eia for Igg Antibody to Ebv Vca in Human SerumGNP · Traditional Granbio, Inc.09/12/1990SE
K883670Serological Test Kit for Igg Anti. Epstein-Barr ViGNP · Traditional Electro-Nucleonics, Inc.04/28/1989SE
K884591Ebv-Vca Antibody (Igg)GNP · Traditional Hillcrest Biologicals01/24/1989SE
K880885Ebv-Vca Igg Antibody Test System (Enzyme)GNP · Traditional Immuno Concepts, Inc.08/30/1988SE
K880883Ebv-Vca Igg Antibody Test System (Fluorescent)GNP · Traditional Immuno Concepts, Inc.08/30/1988SE
K871373Ebv-Check(Tm) Test Kit (Igg)GNP · Traditional Diagnostic Technology, Inc.06/25/1987SE

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Questions and answers

When was Is Ebv-Ea-D Igg Elisa Test System cleared by the FDA?

Is Ebv-Ea-D Igg Elisa Test System (K981831) received a 510(k) decision of Substantially Equivalent on February 16, 1999, 270 days after the submission was received.

What is the product code of K981831?

The FDA product code is GNP – Antiserum, Cf, Epstein-Barr Virus, a Class I (low risk) device regulated under 21 CFR 866.3235.