Quanta Lite B2 Gpi Iga

FDA 510(k) K973006 · Inova Diagnostics, Inc.

Substantially Equivalent

510(k) numberK973006

Submission

Device name
Quanta Lite B2 Gpi Iga
Applicant
Inova Diagnostics, Inc.
San Diego, CA, US
Received
August 13, 1997
Decision date
October 20, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 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 Quanta Lite B2 Gpi Iga cleared by the FDA?

Quanta Lite B2 Gpi Iga (K973006) received a 510(k) decision of Substantially Equivalent on October 20, 1997, 68 days after the submission was received.

What is the product code of K973006?

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.