Cleared Traditional

K923203 - SYSTEMATE CREATININE TEST

K923203 is the FDA 510(k) clearance for SYSTEMATE CREATININE TEST by Em Diagnostic Systems, Inc.. It is a Class 2 Chemistry device (product code CGX) cleared through the Traditional 510(k) pathway after a 76-day FDA review.

K923203 · Em Diagnostic Systems, Inc. · Chemistry device
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Sep 1992
Decision
76d
Days
Class 2
Risk

K923203 is an FDA 510(k) clearance for the SYSTEMATE CREATININE TEST. Classified as Alkaline Picrate, Colorimetry, Creatinine (product code CGX), Class II - Special Controls.

Submitted by Em Diagnostic Systems, Inc. (Gibbstown, US). The FDA issued a Cleared decision on September 9, 1992 after a review of 76 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1225 - 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 K923203 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 25, 1992
Decision Date September 09, 1992
Days to Decision 76 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
12d faster than avg
Panel avg: 88d · This submission: 76d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code CGX Alkaline Picrate, Colorimetry, Creatinine
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1225
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Chemistry devices follow this clearance model.

Regulatory Peers - CGX Alkaline Picrate, Colorimetry, Creatinine

All 110
Devices cleared under the same product code (CGX) and FDA review panel - the closest regulatory comparables to K923203.
OLYMPUS CREATININE REAGENT
K924692 · Olympus Corp. · Oct 1992
CREATININE-IP TEST, # 42375/93, 42323/R1, 42323/R2
K924599 · Em Diagnostic Systems, Inc. · Oct 1992
OLYMPUS CREATININE REAGENT
K923526 · Olympus Corp. · Sep 1992
MILES URINE CREATININE METHOD
K923039 · Heraeus Kulzer, Inc. · Aug 1992
SYNCHRON CREATININE TRIGGERED TEST CX4,5,7,
K915077 · Beckman Instruments, Inc. · Dec 1991
ABBOTT QUICKSTART CREATININE TEST(CREA) ITEM# 5A28
K913707 · Em Diagnostic Systems, Inc. · Sep 1991