Cleared Traditional

K041926 - HDL/LDL-ADVANCE CALIBRATOR

K041926 is the FDA 510(k) clearance for HDL/LDL-ADVANCE CALIBRATOR by Diagnostic Chemicals , Ltd.. It is a Class 2 Chemistry device (product code JIX) cleared through the Traditional 510(k) pathway after a 127-day FDA review.

K041926 · Diagnostic Chemicals , Ltd. · Chemistry device
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Nov 2004
Decision
127d
Days
Class 2
Risk

K041926 is an FDA 510(k) clearance for the HDL/LDL-ADVANCE CALIBRATOR, CAT. NO. SE-278. Classified as Calibrator, Multi-analyte Mixture (product code JIX), Class II - Special Controls.

Submitted by Diagnostic Chemicals , Ltd. (Charlottetown, P.E., CA). The FDA issued a Cleared decision on November 23, 2004 after a review of 127 days - within the typical 510(k) review window.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1150 - 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. devices

Submission Details

510(k) Number K041926 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 19, 2004
Decision Date November 23, 2004
Days to Decision 127 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
39d slower than avg
Panel avg: 88d · This submission: 127d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code JIX Calibrator, Multi-analyte Mixture
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1150
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 - JIX Calibrator, Multi-analyte Mixture

All 201
Devices cleared under the same product code (JIX) and FDA review panel - the closest regulatory comparables to K041926.
LIPOPROTEIN FOR MULTIPLE ANALYTES
K051619 · Bayer Healthcare, LLC · Aug 2005
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K043460 · Olympus America, Inc. · Jan 2005
PRECINORM PROTEINS IN URINE/CSF (PUC) AND PRECIPATH PUC
K050026 · Roche Diagnostics · Jan 2005
MULTI-CHEM CALIBRATOR A
K042551 · Wako Chemicals USA, Inc. · Nov 2004
MULTI CHEM CAL B
K042549 · Wako Chemicals USA, Inc. · Nov 2004
MULTI-LIPID CALIBRATOR
K042550 · Wako Chemicals USA, Inc. · Nov 2004