510(k) K100588

Device
HUMAN IGA2 KIT FOR USE ON THE SPAPLUS
Applicant
THE BINDING SITE GROUP LTD
510(k) number
K100588
Product code
CFN  
Decision
Substantially Equivalent (SESE)
Decision date
2010-08-16
Date received
2010-03-02
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

Related Records

Applicant Contact

Contact
JAY GELLER
Address
12100 Wilshire Bl., Suite 500 Los Angeles CA US 90025 90025

FDA Registration Numbers

Source Documents

510(k) summary PDF not indicated by FDA

Related GUDID Devices

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05051700012317Human IgA1 Kit SPAplusTHE BINDING SITE GROUP LIMITED2016-09-24

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K120901HUMAN IGA CSF KIT FOR USE ON SPAPLUSThe Binding Site Group , Ltd.2013-05-30
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Legacy Summary

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Decision Summary