Synchron CX Systems Gamma-Glutamyl Transferase Reagent (GGT)

FDA 510(k) K971466 · Carolina Liquid Chemistries Corp.

Substantially Equivalent

510(k) numberK971466

Submission

Device name
Synchron CX Systems Gamma-Glutamyl Transferase Reagent (GGT)
Applicant
Carolina Liquid Chemistries Corp.
Brea, CA, US
Received
April 22, 1997
Decision date
May 6, 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
JQB – Kinetic Method, Gamma-Glutamyl Transpeptidase
Device class
Class I (low risk)
Regulation
21 CFR 862.1360
Specialty
Clinical Chemistry

Other 510(k)s with product code JQB

510(k)DeviceApplicantDecision
K974000Y-Glutamyltransferase-Sl Assay , Cataloge Number 324-10, 324-30JQB · Traditional Diagnostic Chemicals , Ltd.11/04/1997SE
K973157Liquid GGT (Gamma Glutamyl Transferase) Reagent SetJQB · Traditional Pointe Scientific, Inc.,10/10/1997SE
K964457Roche Cobas Ibtegra Reagent CassettesJQB · Traditional Roche Diagnostic Systems, Inc.01/13/1997SE
K964916Gamma-Glutamyl TranspeptidaseJQB · Traditional Derma Media Lab., Inc.01/10/1997SE
K955770Gamma Glutamyl Transferase Test SystemJQB · Traditional Abaxis, Inc.09/09/1996SE
K945800Y-Glutamyltransferase Assay, Catalogue Number 308-05JQB · Traditional Diagnostic Chemicals , Ltd.06/09/1995SE
K946192Hichem Y-Gt Reagent KitJQB · Traditional Hichem Diagnostics05/02/1995SE
K942962GGT QvetJQB · Traditional Prisma Systems12/07/1994SE
K935984Glutamyl-Transferase, Procedure No. 419JQB · Traditional Sigma Diagnostics, Inc.07/20/1994SE
K941315Stanbio Y-Gt (Liquicolor) Test SetJQB · Traditional Stanbio Laboratory07/14/1994SE

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Questions and answers

When was Synchron CX Systems Gamma-Glutamyl Transferase Reagent (GGT) cleared by the FDA?

Synchron CX Systems Gamma-Glutamyl Transferase Reagent (GGT) (K971466) received a 510(k) decision of Substantially Equivalent on May 6, 1997, 14 days after the submission was received.

What is the product code of K971466?

The FDA product code is JQB – Kinetic Method, Gamma-Glutamyl Transpeptidase, a Class I (low risk) device regulated under 21 CFR 862.1360.