Elia Gliadin Iga, Igg and Celiac Control

FDA 510(k) K063775 · Phadia US, Inc.

Substantially Equivalent

510(k) numberK063775

Submission

Device name
Elia Gliadin Iga, Igg and Celiac Control
Applicant
Phadia US, Inc.
Portage, MI, US
Received
December 21, 2006
Decision date
March 14, 2007
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MST – Antibodies, Gliadin
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5750
Specialty
Immunology

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K083053Euroimmun Anti-Gliadin (GAF-3X) Elisa (Igg)MST · Traditional Euroimmun Us, Inc.08/07/2009SE
K083052Euroimmun Anti-Gliadin (GAF-3X) Elisa (Iga)MST · Traditional Euroimmun Us, Inc.07/28/2009SE
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K112414Elia B2-GLYCOPROTEIN I Iga ImmunoassayMSV · Traditional 06/22/2012SE
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K102673Rheumatoid Factor Immunological Test SystemDHR · Traditional 09/30/2011SE
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Questions and answers

When was Elia Gliadin Iga, Igg and Celiac Control cleared by the FDA?

Elia Gliadin Iga, Igg and Celiac Control (K063775) received a 510(k) decision of Substantially Equivalent on March 14, 2007, 83 days after the submission was received.

What is the product code of K063775?

The FDA product code is MST – Antibodies, Gliadin, a Class II (moderate risk) device regulated under 21 CFR 866.5750.