Cleared Traditional

K913024 - ABBOTT QUICKSTART GAMMA-GLUTAMYTRANSFER...

K913024 is the FDA 510(k) clearance for ABBOTT QUICKSTART GAMMA-GLUTAMYTRANSFER... by Em Diagnostic Systems, Inc.. It is a Class 1 Chemistry device (product code JQB) cleared through the Traditional 510(k) pathway after a 17-day FDA review.

K913024 · Em Diagnostic Systems, Inc. · Chemistry device
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Jul 1991
Decision
17d
Days
Class 1
Risk

K913024 is an FDA 510(k) clearance for the ABBOTT QUICKSTART GAMMA-GLUTAMYTRANSFERASE TEST. Classified as Kinetic Method, Gamma-glutamyl Transpeptidase (product code JQB), Class I - General Controls.

Submitted by Em Diagnostic Systems, Inc. (Gibbstown, US). The FDA issued a Cleared decision on July 26, 1991 after a review of 17 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 Em Diagnostic Systems, Inc. devices

Submission Details

510(k) Number K913024 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 09, 1991
Decision Date July 26, 1991
Days to Decision 17 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
71d faster than avg
Panel avg: 88d · This submission: 17d
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 K913024.
GAMMA GULTAMYL TRANSFERASE TEST
K922947 · Em Diagnostic Systems, Inc. · Sep 1992
OLYMPUS GGT REAGENT
K922230 · Olympus Corp. · Jun 1992
TRACE GAMMA GT-SS REAGENT
K914731 · Trace Scientific , Ltd. · Nov 1991
SYSTEMATE GGT (EPOS APPLICATION) #65414
K905662 · Em Diagnostic Systems, Inc. · Jan 1991
RAICHEM GGT REAGENT
K905085 · Reagents Applications, Inc. · Dec 1990
GGT REAGENTS, 7738, 7739, 7538, 7438 & 7138
K905096 · Amresco, Inc. · Nov 1990