Cleared Traditional

K860135 - EASY-TEST UREA (BUN) REAGENT

K860135 is the FDA 510(k) clearance for EASY-TEST UREA (BUN) REAGENT by Em Diagnostic Systems, Inc.. It is a Class 2 Chemistry device (product code CDQ) cleared through the Traditional 510(k) pathway after a 38-day FDA review.

K860135 · Em Diagnostic Systems, Inc. · Chemistry device
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Feb 1986
Decision
38d
Days
Class 2
Risk

K860135 is an FDA 510(k) clearance for the EASY-TEST UREA (BUN) REAGENT. Classified as Urease And Glutamic Dehydrogenase, Urea Nitrogen (product code CDQ), Class II - Special Controls.

Submitted by Em Diagnostic Systems, Inc. (Gibbstown, US). The FDA issued a Cleared decision on February 21, 1986 after a review of 38 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 Em Diagnostic Systems, Inc. devices

Submission Details

510(k) Number K860135 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 14, 1986
Decision Date February 21, 1986
Days to Decision 38 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
50d faster than avg
Panel avg: 88d · This submission: 38d
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 87
Devices cleared under the same product code (CDQ) and FDA review panel - the closest regulatory comparables to K860135.
BLOOD UREA NITROGEN (BUN) PROCEDURE
K861666 · Data Medical Associates, Inc. · Jul 1986
UREA NITROGEN (GLDH) REAGENT SET (UV)
K862210 · Sterling Diagnostics, Inc. · Jul 1986
ENZYMATIC BUN REAGENT
K860716 · Trace Scientific , Ltd. · Apr 1986
TDX REA BUN
K853677 · Abbott Laboratories · Sep 1985
UREASE & GLUTAMATE DEHYDROGENASE, UREA NITROGEN
K853102 · Diagnostic Chemicals, Ltd. (Usa) · Aug 1985
DURAZYME UREA NITROGEN
K852292 · American Monitor Corp. · Jul 1985