Cleared Traditional

K923035 - MILES URINE UREA NITROGEN METHOD

K923035 is the FDA 510(k) clearance for MILES URINE UREA NITROGEN METHOD by Heraeus Kulzer, Inc.. It is a Class 2 Chemistry device (product code CDQ) cleared through the Traditional 510(k) pathway after a 82-day FDA review.

K923035 · Heraeus Kulzer, Inc. · Chemistry device
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Sep 1992
Decision
82d
Days
Class 2
Risk

K923035 is an FDA 510(k) clearance for the MILES URINE UREA NITROGEN METHOD. Classified as Urease And Glutamic Dehydrogenase, Urea Nitrogen (product code CDQ), Class II - Special Controls.

Submitted by Heraeus Kulzer, Inc. (Tarrytown, US). The FDA issued a Cleared decision on September 9, 1992 after a review of 82 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1770 - 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 Heraeus Kulzer, Inc. devices

Submission Details

510(k) Number K923035 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 19, 1992
Decision Date September 09, 1992
Days to Decision 82 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
6d faster than avg
Panel avg: 88d · This submission: 82d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code CDQ Urease And Glutamic Dehydrogenase, Urea Nitrogen
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1770
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 - CDQ Urease And Glutamic Dehydrogenase, Urea Nitrogen

All 90
Devices cleared under the same product code (CDQ) and FDA review panel - the closest regulatory comparables to K923035.
OLYMPUS REPLY UREA NITROGEN REAGENT
K931745 · Olympus Corp. · Aug 1993
UREA NITROGEN TEST
K925002 · Em Diagnostic Systems, Inc. · Jan 1993
OLYMPUS BUN REAGENT
K924693 · Olympus Corp. · Nov 1992
OLYMPUS UREA NITROGEN (BUN) REAGENT
K922597 · Olympus Corp. · Jul 1992
IL TEST(TM) UREA NITROGEN
K914877 · Instrumentation Laboratory CO · Mar 1992
SYNERMED UREA NITROGEN REAGENT KIT
K911248 · Synermed, Inc. · Jun 1991