Cleared Traditional

K861660 - URIC ACID PROCEDURE

K861660 is the FDA 510(k) clearance for URIC ACID PROCEDURE by Data Medical Associates, Inc.. It is a Class 1 Chemistry device (product code KNK) cleared through the Traditional 510(k) pathway after a 44-day FDA review.

K861660 · Data Medical Associates, Inc. · Chemistry device
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Jun 1986
Decision
44d
Days
Class 1
Risk

K861660 is an FDA 510(k) clearance for the URIC ACID PROCEDURE. Classified as Acid, Uric, Uricase (colorimetric) (product code KNK), Class I - General Controls.

Submitted by Data Medical Associates, Inc. (Arlington, US). The FDA issued a Cleared decision on June 13, 1986 after a review of 44 days - a notably fast clearance cycle.

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: 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 Data Medical Associates, Inc. devices

Submission Details

510(k) Number K861660 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 30, 1986
Decision Date June 13, 1986
Days to Decision 44 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
44d faster than avg
Panel avg: 88d · This submission: 44d
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 79
Devices cleared under the same product code (KNK) and FDA review panel - the closest regulatory comparables to K861660.
URICMETER
K863113 · J. D. Assoc. · Sep 1986
REFLOTRON URIC ACID
K861831 · Boehringer Mannheim Corp. · Jul 1986
KING DIAGNOSTICS URIC ACID TEST
K862208 · King Diagnostics, Inc. · Jul 1986
ENZYMATIC URIC ACID REAGENT
K860732 · Trace Scientific , Ltd. · Apr 1986
EASY-TEST URIC ACID (URIC), #67516/93
K860916 · Em Diagnostic Systems, Inc. · Apr 1986
URIC ACID REAGNET SET (TRINDER)
K860477 · Sterling Diagnostics, Inc. · Apr 1986