Theratest EL-BETA2GPI (Igm-Igg-Iga), Theratest EL--BETA2GPI SCR

FDA 510(k) K092757 · Thera-Test Laboratories, Inc.

Substantially Equivalent

510(k) numberK092757

Submission

Device name
Theratest EL-BETA2GPI (Igm-Igg-Iga), Theratest EL--BETA2GPI SCR
Applicant
Thera-Test Laboratories, Inc.
Lombard, IL, US
Received
September 9, 2009
Decision date
October 9, 2009
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
MSV – System,Test,Antibodies,B2 - Glycoprotein I (B2 - Gpi)
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5660
Specialty
Immunology

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Questions and answers

When was Theratest EL-BETA2GPI (Igm-Igg-Iga), Theratest EL--BETA2GPI SCR cleared by the FDA?

Theratest EL-BETA2GPI (Igm-Igg-Iga), Theratest EL--BETA2GPI SCR (K092757) received a 510(k) decision of Substantially Equivalent on October 9, 2009, 30 days after the submission was received.

What is the product code of K092757?

The FDA product code is MSV – System,Test,Antibodies,B2 - Glycoprotein I (B2 - Gpi), a Class II (moderate risk) device regulated under 21 CFR 866.5660.