Cleared Traditional

K860723 - G.T. (GAMMA-GLUTAMYL TRANSFERASE) REAGENT

K860723 is the FDA 510(k) clearance for G.T. (GAMMA-GLUTAMYL TRANSFERASE) REAGENT by Trace Scientific , Ltd.. It is a Class 1 Chemistry device (product code JPZ) cleared through the Traditional 510(k) pathway after a 40-day FDA review.

K860723 · Trace Scientific , Ltd. · Chemistry device
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Apr 1986
Decision
40d
Days
Class 1
Risk

K860723 is an FDA 510(k) clearance for the G.T. (GAMMA-GLUTAMYL TRANSFERASE) REAGENT. Classified as Colorimetric Method, Gamma-glutamyl Transpeptidase (product code JPZ), Class I - General Controls.

Submitted by Trace Scientific , Ltd. (Clayton, Vic 3168, AU). The FDA issued a Cleared decision on April 7, 1986 after a review of 40 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1360 - the FDA in vitro diagnostics and chemistry framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Trace Scientific , Ltd. devices

Submission Details

510(k) Number K860723 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 26, 1986
Decision Date April 07, 1986
Days to Decision 40 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
48d faster than avg
Panel avg: 88d · This submission: 40d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JPZ Colorimetric Method, Gamma-glutamyl Transpeptidase
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.1360
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - JPZ Colorimetric Method, Gamma-glutamyl Transpeptidase

All 20
Devices cleared under the same product code (JPZ) and FDA review panel - the closest regulatory comparables to K860723.
VISION (TM) GGTP
K864208 · Abbott Laboratories · Nov 1986
GAMMA GLUTAMYL TRANSFERASE PROCEDURE
K863586 · Data Medical Associates, Inc. · Oct 1986
GAMMA GLUTAMYL TRANSFERASE PROCEDURE
K861672 · Data Medical Associates, Inc. · May 1986
GAMMA GLUTAMYL TRANSPEPTIDASE (GGTP) REAGENT SET
K860348 · Sterling Diagnostics, Inc. · Mar 1986
GLUTAMYLTRANSFERASE ASSAY KIT
K850788 · Diagnostic Chemicals, Ltd. (Usa) · Mar 1985
WAKO R-GTP C-TEST
K831639 · Wako Chemicals USA, Inc. · Jul 1983