Cleared Traditional

K923765 - SYSTEMATE URICACID TEST

K923765 is the FDA 510(k) clearance for SYSTEMATE URICACID TEST by Em Diagnostic Systems, Inc.. It is a Class 1 Chemistry device (product code CDO) cleared through the Traditional 510(k) pathway after a 56-day FDA review.

K923765 · Em Diagnostic Systems, Inc. · Chemistry device
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Sep 1992
Decision
56d
Days
Class 1
Risk

K923765 is an FDA 510(k) clearance for the SYSTEMATE URICACID TEST, TECHNICON RA 1000. Classified as Acid, Uric, Uricase (u.v.) (product code CDO), Class I - General Controls.

Submitted by Em Diagnostic Systems, Inc. (Gibbstown, US). The FDA issued a Cleared decision on September 22, 1992 after a review of 56 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 Em Diagnostic Systems, Inc. devices

Submission Details

510(k) Number K923765 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 28, 1992
Decision Date September 22, 1992
Days to Decision 56 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
32d faster than avg
Panel avg: 88d · This submission: 56d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code CDO Acid, Uric, Uricase (u.v.)
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 - CDO Acid, Uric, Uricase (u.v.)

All 22
Devices cleared under the same product code (CDO) and FDA review panel - the closest regulatory comparables to K923765.
URIC ACID
K981189 · Abbott Laboratories · May 1998
OLYMPUS URIC ACID REAGENT
K955752 · Olympus America, Inc. · Jan 1996
URIC ACID TEST ITEM NUMBER 65422
K932162 · Em Diagnostic Systems, Inc. · Sep 1993
SYSTEMATE URIC ACID (URCA) ITEM NUMBER 65422
K903335 · Em Diagnostic Systems, Inc. · Aug 1990
BIOTROL URIC ACID ENZYMATIQUE UV H.P.
K875320 · Biotrol, USA, Inc. · Feb 1988
GEMENI URIC ACID U.V.
K873358 · Electro-Nucleonics Laboratories, Inc. · Sep 1987