Cleared Traditional

K855186 - GAMMA GLUTAMYL TRANSPEPTIDASE (KINECTIC)REAGENTSET

K855186 is an FDA 510(k) clearance for GAMMA GLUTAMYL TRANSPEPTIDASE (KINECTIC..., manufactured by Technostics Intl.. The device is a Class 1 Chemistry device with product code JPZ cleared through the Traditional 510(k) pathway after a 19-day FDA review.

K855186 · Technostics Intl. · Chemistry device
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Jan 1986
Decision
19d
Days
Class 1
Risk

K855186 is an FDA 510(k) clearance for the GAMMA GLUTAMYL TRANSPEPTIDASE (KINECTIC)REAGENTSET. Classified as Colorimetric Method, Gamma-glutamyl Transpeptidase (product code JPZ), Class I - General Controls.

Submitted by Technostics Intl. (Washington, US). The FDA issued a Cleared decision on January 14, 1986 after a review of 19 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 Technostics Intl. devices

FDA 510(k) Submission Details - K855186

510(k) Number K855186 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 26, 1985
Decision Date January 14, 1986
Days to Decision 19 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
69d faster than avg
Panel avg: 88d · This submission: 19d
Pathway characteristics
Predicate-based equivalence.

JPZ Device Classification - Class 1, General Controls

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 27
Devices cleared under the same product code (JPZ) and FDA review panel - the closest regulatory comparables to K855186.
G.T. (GAMMA-GLUTAMYL TRANSFERASE) REAGENT
K860723 · Trace Scientific , Ltd. · Apr 1986
GAMMA GLUTAMYL TRANSPEPTIDASE (GGTP) REAGENT SET
K860348 · Sterling Diagnostics, Inc. · Mar 1986
GAMMA GLUTAMYL TRANSPEPTIDASE REAGENT SET
K855156 · Technostics Intl. · Jan 1986
GLUTAMYLTRANSFERASE ASSAY KIT
K850788 · Diagnostic Chemicals, Ltd. (Usa) · Mar 1985
WAKO R-GTP C-TEST
K831639 · Wako Chemicals USA, Inc. · Jul 1983
RAICHEM & GT REAGENT
K823090 · Reagents Applications, Inc. · Nov 1982