Cleared Traditional

K881626 - GAMMA-GLUTAMYL TRANSFERASE

K881626 is the FDA 510(k) clearance for GAMMA-GLUTAMYL TRANSFERASE by Tech-Co, Inc.. It is a Class 1 Chemistry device (product code JQB) cleared through the Traditional 510(k) pathway after a 45-day FDA review.

K881626 · Tech-Co, Inc. · Chemistry device
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May 1988
Decision
45d
Days
Class 1
Risk

K881626 is an FDA 510(k) clearance for the GAMMA-GLUTAMYL TRANSFERASE. Classified as Kinetic Method, Gamma-glutamyl Transpeptidase (product code JQB), Class I - General Controls.

Submitted by Tech-Co, Inc. (Oak Park, US). The FDA issued a Cleared decision on May 27, 1988 after a review of 45 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 Tech-Co, Inc. devices

Submission Details

510(k) Number K881626 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 12, 1988
Decision Date May 27, 1988
Days to Decision 45 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
43d faster than avg
Panel avg: 88d · This submission: 45d
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 K881626.
GAMMA GLUTAMYL TRANSFERASE TEST, ITEM: 65414/R1
K893765 · Em Diagnostic Systems, Inc. · Jul 1989
GAMMA-GLUTAMYLTRANSFERASE
K890312 · American Monitor Corp. · Mar 1989
GAMMA GLUTAMYL TRANSFERASE TEST (GGT) ITEM: 65664
K884988 · Em Diagnostic Systems, Inc. · Jan 1989
BIOTROL -GT GAMMA-GLUTAMYL TRANSFERASE (GGT) TEST
K881311 · Biotrol, USA, Inc. · Apr 1988
GAMMA GLUTAMYLTRANSFERASE
K873378 · Catachem, Inc. · Sep 1987
UNIFAST GAMMA-GT
K873135 · Sclavo, Inc. · Sep 1987