Diagnostic METHOD-8-GLUTAMYLTRANSFERASE

FDA 510(k) K761090 · Technicon Instruments Corp.

Substantially Equivalent

510(k) numberK761090

Submission

Device name
Diagnostic METHOD-8-GLUTAMYLTRANSFERASE
Applicant
Technicon Instruments Corp.
Mchenry, IL, US
Received
November 22, 1976
Decision date
December 2, 1976
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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 Diagnostic METHOD-8-GLUTAMYLTRANSFERASE cleared by the FDA?

Diagnostic METHOD-8-GLUTAMYLTRANSFERASE (K761090) received a 510(k) decision of Substantially Equivalent on December 2, 1976, 10 days after the submission was received.

What is the product code of K761090?

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