Cleared Traditional

K790812 - COULTER ACCU-ZYME IIY-GT REAGENT KIT

K790812 is an FDA 510(k) clearance for COULTER ACCU-ZYME IIY-GT REAGENT KIT, manufactured by Coulter Electronics, Inc.. The device is a Class 1 Chemistry device with product code JPZ cleared through the Traditional 510(k) pathway after a 63-day FDA review.

K790812 · Coulter Electronics, Inc. · Chemistry device
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Jun 1979
Decision
63d
Days
Class 1
Risk

K790812 is an FDA 510(k) clearance for the COULTER ACCU-ZYME IIY-GT REAGENT KIT. Classified as Colorimetric Method, Gamma-glutamyl Transpeptidase (product code JPZ), Class I - General Controls.

Submitted by Coulter Electronics, Inc. (Mchenry, US). The FDA issued a Cleared decision on June 28, 1979 after a review of 63 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 Coulter Electronics, Inc. devices

FDA 510(k) Submission Details - K790812

510(k) Number K790812 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 26, 1979
Decision Date June 28, 1979
Days to Decision 63 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
25d faster than avg
Panel avg: 88d · This submission: 63d
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 K790812.
GILCHEM Y-GT REAGENT
K822149 · Gilford Diagnostics · Aug 1982
ULTRAZYME PLUS 2GT
K821871 · Harleco Diagnostics · Jul 1982
ULTRAZYME PLUS-GT, #64959 & 65032
K821468 · Emd Chemicals, Inc. · Jun 1982
SMA/GGT
K781533 · Technicon Instruments Corp. · Oct 1978
ULTRAZYME PLUS GT
K780099 · Harleco · Mar 1978
REAGENT SYSTEM (NO. SC 135)
K760711 · Sigma Chemical Co. · Nov 1976