Cleared Traditional

K861700 - DIMENSION (TM) CLINICAL CHEMISTRY SYSTEM

K861700 is the FDA 510(k) clearance for DIMENSION (TM) CLINICAL CHEMISTRY SYSTEM by E.I. Dupont DE Nemours & Co., Inc.. It is a Class 1 Chemistry device (product code CHH) cleared through the Traditional 510(k) pathway after a 37-day FDA review.

K861700 · E.I. Dupont DE Nemours & Co., Inc. · Chemistry device
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Jun 1986
Decision
37d
Days
Class 1
Risk

K861700 is an FDA 510(k) clearance for the DIMENSION (TM) CLINICAL CHEMISTRY SYSTEM. Classified as Enzymatic Esterase--oxidase, Cholesterol (product code CHH), Class I - General Controls.

Submitted by E.I. Dupont DE Nemours & Co., Inc. (Wilmington, US). The FDA issued a Cleared decision on June 11, 1986 after a review of 37 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1175 - 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 E.I. Dupont DE Nemours & Co., Inc. devices

Submission Details

510(k) Number K861700 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 05, 1986
Decision Date June 11, 1986
Days to Decision 37 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
51d faster than avg
Panel avg: 88d · This submission: 37d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code CHH Enzymatic Esterase--oxidase, Cholesterol
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.1175
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 - CHH Enzymatic Esterase--oxidase, Cholesterol

All 126
Devices cleared under the same product code (CHH) and FDA review panel - the closest regulatory comparables to K861700.
EMDS(TM) CHOLESTEROL TESTPACK, # 67685/95
K862707 · Em Diagnostic Systems, Inc. · Aug 1986
FAST CHOLESTEROL (TOTAL CHOLESTEROL TEST)
K862507 · Sclavo, Inc. · Jul 1986
CHOLESTEROL PROCEDURE
K861659 · Data Medical Associates, Inc. · Jun 1986
ENZYMATIC CHOLESTEROL REAGENT (SINGLE VIAL)
K860717 · Trace Scientific , Ltd. · Apr 1986
TOTAL CHOLESTEROL REAGENT SET
K855028 · Sterling Diagnostics, Inc. · Jan 1986
KODAK EKTACHEM HDL CHOLESTEROL KIT
K854426 · Eastman Kodak Company · Jan 1986