Stanbio Y-Gt (Liquicolor) Test Set

FDA 510(k) K941315 · Stanbio Laboratory

Substantially Equivalent

510(k) numberK941315

Submission

Device name
Stanbio Y-Gt (Liquicolor) Test Set
Applicant
Stanbio Laboratory
San Antonio, TX, US
Received
March 18, 1994
Decision date
July 14, 1994
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
K971466Synchron CX Systems Gamma-Glutamyl Transferase Reagent (GGT)JQB · Traditional Carolina Liquid Chemistries Corp.05/06/1997SE
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

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Questions and answers

When was Stanbio Y-Gt (Liquicolor) Test Set cleared by the FDA?

Stanbio Y-Gt (Liquicolor) Test Set (K941315) received a 510(k) decision of Substantially Equivalent on July 14, 1994, 118 days after the submission was received.

What is the product code of K941315?

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