Cleared Traditional

K932766 - HDL-CHOLESTRAL(DEXTRAN SULFATE/MAGNESIUM)

K932766 is an FDA 510(k) clearance for HDL-CHOLESTRAL(DEXTRAN SULFATE/MAGNESIUM), manufactured by Diagnostic Chemicals, Ltd. (Usa). The device is a Class 1 Chemistry device with product code LBR cleared through the Traditional 510(k) pathway after a 185-day FDA review.

K932766 · Diagnostic Chemicals, Ltd. (Usa) · Chemistry device
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Dec 1993
Decision
185d
Days
Class 1
Risk

K932766 is an FDA 510(k) clearance for the HDL-CHOLESTRAL(DEXTRAN SULFATE/MAGNESIUM). Classified as Ldl & Vldl Precipitation, Hdl (product code LBR), Class I - General Controls.

Submitted by Diagnostic Chemicals, Ltd. (Usa) (Charlottestown,Pei,Canada, CA). The FDA issued a Cleared decision on December 10, 1993 after a review of 185 days - an extended review cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1475 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Chemistry review framework, consistent with the majority of Class II 510(k) submissions.

View all Diagnostic Chemicals, Ltd. (Usa) devices

FDA 510(k) Submission Details - K932766

510(k) Number K932766 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 08, 1993
Decision Date December 10, 1993
Days to Decision 185 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
97d slower than avg
Panel avg: 88d · This submission: 185d
Pathway characteristics
Predicate-based equivalence.

LBR Device Classification - Class 1, General Controls

Product Code LBR Ldl & Vldl Precipitation, Hdl
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.1475
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 - LBR Ldl & Vldl Precipitation, Hdl

All 53
Devices cleared under the same product code (LBR) and FDA review panel - the closest regulatory comparables to K932766.
N-GENEOUS HDL CHOLESTEROL KIT/CHOLESTEROL CALIBRATOR
K962186 · Genzyme Corp. · Aug 1996
HDL PRECIPITATING REAGENT
K954179 · Schiapparelli Biosystems, Inc. · Dec 1995
MAGNETIC HDL CHOLESTEROL TEST
K944975 · Reference Diagnostics, Inc. · Aug 1995
INTERSECT SYSTEMS HDL CHOLESTEROL REAGENT SET
K934039 · Intersect Systems, Inc. · Nov 1993
HDL PRECIPITATING REAGENT (DEXTRAN SULFATE)
K931773 · King Diagnostics, Inc. · Aug 1993
SYNERMED HDL CHOLESTLEROL REAGENT KIT
K924427 · Synermed, Inc. · Nov 1992