Cleared Traditional

K843334 - SYSTEMATE GPT 67209

K843334 is the FDA 510(k) clearance for SYSTEMATE GPT 67209 by Em Diagnostic Systems, Inc.. It is a Class 1 Chemistry device (product code CKA) cleared through the Traditional 510(k) pathway after a 24-day FDA review.

K843334 · Em Diagnostic Systems, Inc. · Chemistry device
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Sep 1984
Decision
24d
Days
Class 1
Risk

K843334 is an FDA 510(k) clearance for the SYSTEMATE GPT 67209. Classified as Nadh Oxidation/nad Reduction, Alt/sgpt (product code CKA), Class I - General Controls.

Submitted by Em Diagnostic Systems, Inc. (Walker, US). The FDA issued a Cleared decision on September 20, 1984 after a review of 24 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1030 - 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 K843334 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 27, 1984
Decision Date September 20, 1984
Days to Decision 24 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
64d faster than avg
Panel avg: 88d · This submission: 24d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code CKA Nadh Oxidation/nad Reduction, Alt/sgpt
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.1030
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 - CKA Nadh Oxidation/nad Reduction, Alt/sgpt

All 98
Devices cleared under the same product code (CKA) and FDA review panel - the closest regulatory comparables to K843334.
HI-CHEM DIAGNOSTICS ENZYME RINSE CONCENTRATE
K852867 · Hi Chem, Inc. · Aug 1985
AMRESCO FLOW PAC SMA PHOSPHATE BUFFER CONCENTRATE
K851923 · Amresco, Inc. · May 1985
ROCHE REAGENT FOR ALT
K843111 · Roche Diagnostic Systems, Inc. · Oct 1984
SIGMA 59-UV FOR ALANINE AMINOTRANSFER
K842564 · Sigma Chemical Co. · Aug 1984
ALANINE AMINOTRANSFERASE ASSAY KIT
K842241 · Diagnostic Chemicals, Ltd. (Usa) · Jul 1984
SGPT REAGENT SET
K841060 · Medical Specialties, Inc. · May 1984