510(k) K972295

Device
SERAQUEST VZV IGG
Applicant
QUEST INTL., INC.
510(k) number
K972295
Product code
LFY  
Decision
Substantially Equivalent (SESE)
Decision date
1997-11-05
Date received
1997-06-19
Regulation
866.3900
Classification name
Enzyme Linked Immunoabsorbent Assay, Varicella-zoster
Medical specialty
Microbiology
Review panel
Microbiology
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
ROBERT A CORT
Address
1938 NE 148th Terr. North Miami FL US 33181 33181

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code LFY  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K231214LIAISON VZV IgG HT, LIAISON Control VZV IgG HTDiaSorin, Inc.2023-10-27
K150375LIAISON VZV IgG, LIAISON Control VZV IgGDiaSorin, Inc.2015-03-11
K070317ZEUS SCIENTIFIC, INC VZV IGM ELISA TEST SYSTEMZeus Scientific, Inc.2007-07-05
K061820DIASORIN LIAISON VZV IGGDiaSorin, Inc.2007-02-26
K051484ZEUS SCIENTIFIC, INC., ATHENA MULTI-LYTE MMRV IGG TEST SYSTEM.Zeus Scientific, Inc.2005-12-05
K984181THE APTUS (AUTOMATED) APPLICATION OF THE VZV IGG ELISA TEST SYSTEMZeus Scientific, Inc.1999-01-22
K981867IS-VZU IGG TEST SYSTEMDiamedix Corp.1998-09-28
K961012VZV IGG ELISA TEST SYSTEMZeus Scientific, Inc.1996-07-24
K943843VARICELISA, MODIFICATIONBiowhittaker Molecular Applications, Inc.1996-03-14
K941046VZV IGG ELISA TESTGull Laboratories, Inc.1995-08-24
K923122VITEK IMMUNODIAGNOSTIC ASSAY SYSTEMBiomerieux Vitek, Inc.1992-10-26
K914022SERIOLOGICAL TEST KIT/IGM ANTIBODY VARI-ZOST VIRUSPharmacia Diagnostics, Inc.1992-01-27
K900688VARICELLA ZOSTER IGG CLIN-ELISA TEST KITClinical Sciences, Inc.1990-05-15
K890642VZV MICROASSAYDiamedix Corp.1989-05-15
K833637VZV BIO-ENZABEAD SCREEN KITBionetic Laboratory Products1984-02-10

Legacy Summary#

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FDA Review#

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