Cleared Traditional

K961586 - URIC ACID-SL ASSAY CATALOGUE NO. 237-60

K961586 is the FDA 510(k) clearance for URIC ACID-SL ASSAY CATALOGUE NO. 237-60 by Diagnostic Chemicals , Ltd.. It is a Class 1 Chemistry device (product code KNK) cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K961586 · Diagnostic Chemicals , Ltd. · Chemistry device
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Jul 1996
Decision
90d
Days
Class 1
Risk

K961586 is an FDA 510(k) clearance for the URIC ACID-SL ASSAY CATALOGUE NO. 237-60. Classified as Acid, Uric, Uricase (colorimetric) (product code KNK), Class I - General Controls.

Submitted by Diagnostic Chemicals , Ltd. (Charlottetown, P.E.I., CA). The FDA issued a Cleared decision on July 23, 1996 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1775 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Chemistry review framework, consistent with the majority of Class II 510(k) submissions.

View all Diagnostic Chemicals , Ltd. devices

Submission Details

510(k) Number K961586 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 24, 1996
Decision Date July 23, 1996
Days to Decision 90 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
2d slower than avg
Panel avg: 88d · This submission: 90d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KNK Acid, Uric, Uricase (colorimetric)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.1775
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 - KNK Acid, Uric, Uricase (colorimetric)

All 78
Devices cleared under the same product code (KNK) and FDA review panel - the closest regulatory comparables to K961586.
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URIC ACID CATALOGE# 220-93/94/97
K955496 · Diagnostic Chemicals , Ltd. · Feb 1996
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K932728 · Eastman Kodak Company · Apr 1994
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K931350 · Instrumentation Laboratory CO · Oct 1993