Varicella-Zoster Virus Antibody Test Kit-Latex Agg

FDA 510(k) K903882 · Viral Antigens, Inc.

Substantially Equivalent

510(k) numberK903882

Submission

Device name
Varicella-Zoster Virus Antibody Test Kit-Latex Agg
Applicant
Viral Antigens, Inc.
Memphis, TN, US
Received
August 22, 1990
Decision date
December 4, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GQW – Antigen, Cf, (Including Cf Control), Varicella-Zoster
Device class
Class II (moderate risk)
Regulation
21 CFR 866.3900
Specialty
Microbiology

Other 510(k)s with product code GQW

510(k)DeviceApplicantDecision
K070206Diagnostic Hybrids D3 Dfa Varicella-Zoster Virus Identification Kit, 01-020000GQW · Traditional Diagnostic Hybrids, Inc.08/30/2007SE
K990141Light Diagnostics Simulfluor Hsv/Vzv Immunoflourescence Assay, Model 3295GQW · Traditional Light Diagnostics10/19/1999SE
K964872VZV Antigen Control SlidesGQW · Traditional Viral Antigens, Inc.03/18/1997SE
K942743Viro Varicella-Zoster Virus Identification ReagentGQW · Traditional Viro Research, Inc.12/15/1994SE
K912239Vzvscan(Tm) Latex Aggutination TestGQW · Traditional Bd Becton Dickinson Vacutainer Systems Preanalytic06/11/1991SE
K894622Varicella Zoster VirusGQW · Traditional Bion Ent., Ltd.10/24/1989SE
K843676Varicella/Zoster VirusGQW · Traditional Institute Virion , Ltd.09/26/1985SE
K841434Varicella-Zoster(Igg) Ifa TestGQW · Traditional Zeus Scientific, Inc.04/19/1985SE
K802938Varicella-Zoster Antigens & ControlsGQW · Traditional Orion Diagnostica, Inc.12/31/1980SE

More from Orion Diagnostica, Inc.

510(k)DeviceDecision
K971101HSV-2 Antigen Control SlidesGQN · Traditional 07/01/1997SE
K964874HSV-1 Antigen Control SlidesGQN · Traditional 07/01/1997SE
K964875CMV Antigen Control SlidesGQH · Traditional 03/18/1997SE
K964872VZV Antigen Control SlidesGQW · Traditional 03/18/1997SE
K964870RSV Antigen Control SlidesGQG · Traditional 03/18/1997SE

Questions and answers

When was Varicella-Zoster Virus Antibody Test Kit-Latex Agg cleared by the FDA?

Varicella-Zoster Virus Antibody Test Kit-Latex Agg (K903882) received a 510(k) decision of Substantially Equivalent on December 4, 1990, 104 days after the submission was received.

What is the product code of K903882?

The FDA product code is GQW – Antigen, Cf, (Including Cf Control), Varicella-Zoster, a Class II (moderate risk) device regulated under 21 CFR 866.3900.