510(k) K022083

Device
HUMAN IGG SUBCLASS KIT FOR USE ON THE BECKMAN IMMAGE ANALYSER
Applicant
THE BINDING SITE, LTD.
510(k) number
K022083
Product code
CFN  
Decision
Substantially Equivalent (SESE)
Decision date
2002-07-16
Date received
2002-06-26
Regulation
866.5510
Classification name
Method, Nephelometric, Immunoglobulins (g, A, M)
Medical specialty
Immunology
Review panel
Immunology
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
JAY H GELLER
Address
West Tower, Suite 4000 2425 W. Olympic Blvd. Santa Monica CA US 90404 90404

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code CFN  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K233663N Antisera to Human Immunoglobulins (IgG, IgA, and IgM)Siemens Healthcare Diagnostics Products GmbH2023-12-13
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K191985Optilite IgA KitThe Binding Site Group , Ltd.2019-08-19
K191635Optilite IgM KitThe Binding Site Group , Ltd.2019-07-15
K191465Human IgM Kit for use on SPAPlusThe Binding Site Group , Ltd.2019-06-27
K190686Optilite IgM CSF KitThe Binding Site Group , Ltd.2019-05-28
K183151Optilite IgA CSF KitThe Binding Site Group , Ltd.2019-01-23
K162208DxC 700 AU Clinical Chemistry Analyzer, AU IgG ReagentBeckman Coulter, Inc.2017-01-09
K150526Optilite IgG4 KitThe Binding Site Group , Ltd.2015-05-30
K142735The Optilite IgG3 kitThe Binding Site Group , Ltd.2014-12-21
K130122BECKMAN COULTER IMMAGE IMMUNOCHEMISTRY SYSTEM LOW CONCENTRATION IMMUNOGLOBULIN, BECKMAN COULTERBeckman Coulter, Inc.2014-01-07
K120901HUMAN IGA CSF KIT FOR USE ON SPAPLUSThe Binding Site Group , Ltd.2013-05-30
K120750HUMAN IGM CSF KITThe Binding Site Group , Ltd.2013-05-17
K120749HUMAN IGG CSF KITThe Binding Site Group , Ltd.2013-05-17

Legacy Summary#

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FDA Review#

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