Cleared Traditional

K873456 - PARAMAX URIC ACID REAGENT

K873456 is the FDA 510(k) clearance for PARAMAX URIC ACID REAGENT by Baxter Healthcare Corp. It is a Class 1 Chemistry device (product code KNK) cleared through the Traditional 510(k) pathway after a 87-day FDA review.

K873456 · Baxter Healthcare Corp · Chemistry device
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Nov 1987
Decision
87d
Days
Class 1
Risk

K873456 is an FDA 510(k) clearance for the PARAMAX URIC ACID REAGENT. Classified as Acid, Uric, Uricase (colorimetric) (product code KNK), Class I - General Controls.

Submitted by Baxter Healthcare Corp (Santa Ana, US). The FDA issued a Cleared decision on November 23, 1987 after a review of 87 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 Baxter Healthcare Corp devices

Submission Details

510(k) Number K873456 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 28, 1987
Decision Date November 23, 1987
Days to Decision 87 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
1d faster than avg
Panel avg: 88d · This submission: 87d
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 82
Devices cleared under the same product code (KNK) and FDA review panel - the closest regulatory comparables to K873456.
URIC ACID REAGENT (PRODUCT #88219)
K883404 · Hichem Diagnostics · Sep 1988
BIOTROL URIC ACID ENZYMATIQUE TRINDER
K883428 · Biotrol, USA, Inc. · Sep 1988
WAKO AUTOKIT URIC ACID
K880731 · Wako Chemicals USA, Inc. · Mar 1988
URIC ACID PAP
K873363 · Boehringer Mannheim Corp. · Oct 1987
TECHNICON RA(R) SYSTEMS & ASSIST(R) CLIN. ANALYZER
K871892 · Technicon Instruments Corp. · Jun 1987
EASY-TEST URIC ACID (URIC) #16606
K870868 · Em Diagnostic Systems, Inc. · Mar 1987