Cleared Traditional

K890312 - GAMMA-GLUTAMYLTRANSFERASE

K890312 is the FDA 510(k) clearance for GAMMA-GLUTAMYLTRANSFERASE by American Monitor Corp.. It is a Class 1 Chemistry device (product code JQB) cleared through the Traditional 510(k) pathway after a 60-day FDA review.

K890312 · American Monitor Corp. · Chemistry device
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Mar 1989
Decision
60d
Days
Class 1
Risk

K890312 is an FDA 510(k) clearance for the GAMMA-GLUTAMYLTRANSFERASE. Classified as Kinetic Method, Gamma-glutamyl Transpeptidase (product code JQB), Class I - General Controls.

Submitted by American Monitor Corp. (Indianapolis, US). The FDA issued a Cleared decision on March 24, 1989 after a review of 60 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 American Monitor Corp. devices

Submission Details

510(k) Number K890312 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 23, 1989
Decision Date March 24, 1989
Days to Decision 60 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
28d faster than avg
Panel avg: 88d · This submission: 60d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JQB Kinetic 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 - JQB Kinetic Method, Gamma-glutamyl Transpeptidase

All 44
Devices cleared under the same product code (JQB) and FDA review panel - the closest regulatory comparables to K890312.
GGT REAGENTS, 7738, 7739, 7538, 7438 & 7138
K905096 · Amresco, Inc. · Nov 1990
COULTER GAMMA-GT (GGT) REAGENT
K901264 · Coulter Corp. · Apr 1990
GAMMA GLUTAMYL TRANSFERASE TEST, ITEM: 65414/R1
K893765 · Em Diagnostic Systems, Inc. · Jul 1989
GAMMA GLUTAMYL TRANSFERASE TEST (GGT) ITEM: 65664
K884988 · Em Diagnostic Systems, Inc. · Jan 1989
GAMMA-GLUTAMYL TRANSFERASE
K881626 · Tech-Co, Inc. · May 1988
BIOTROL -GT GAMMA-GLUTAMYL TRANSFERASE (GGT) TEST
K881311 · Biotrol, USA, Inc. · Apr 1988