Cleared Traditional

K090209 - HEMOSIL LIQUID HEPARIN

K090209 is the FDA 510(k) clearance for HEMOSIL LIQUID HEPARIN by Instrumentation Laboratory CO. It is a Class 2 Hematology device (product code KFF) cleared through the Traditional 510(k) pathway after a 125-day FDA review.

K090209 · Instrumentation Laboratory CO · Hematology device
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Jun 2009
Decision
125d
Days
Class 2
Risk

K090209 is an FDA 510(k) clearance for the HEMOSIL LIQUID HEPARIN, HEPARIN CALIBRATORS AND LMW AND UF HEPARIN CONTROLS. Classified as Assay, Heparin (product code KFF), Class II - Special Controls.

Submitted by Instrumentation Laboratory CO (Bedford, US). The FDA issued a Cleared decision on June 2, 2009 after a review of 125 days - within the typical 510(k) review window.

This device falls under the Hematology FDA review panel, regulated under 21 CFR 864.7525 - the FDA hematology device 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 Hematology review framework, consistent with the majority of Class II 510(k) submissions.

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Submission Details

510(k) Number K090209 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 28, 2009
Decision Date June 02, 2009
Days to Decision 125 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
12d slower than avg
Panel avg: 113d · This submission: 125d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KFF Assay, Heparin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 864.7525
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 Hematology devices follow this clearance model.

Regulatory Peers - KFF Assay, Heparin

All 22
Devices cleared under the same product code (KFF) and FDA review panel - the closest regulatory comparables to K090209.
HemosIL Liquid Anti-Xa
K213464 · Instrumentation Laboratory CO · Oct 2022
COAMATIC HEPARIN
K983178 · Instrumentation Laboratory CO · Nov 1998
IL TEST HEPARIN
K980242 · Instrumentation Laboratory CO · Mar 1998
MDA HEPARIN ANTI-X ASSAY
K965076 · Organon Teknika Corp. · Mar 1997
CHROM Z-HEPARIN, CAT. NO 5242
K952667 · Helena Laboratories · Feb 1996
THE HEPANORM HBPM/LMWH KIT
K943514 · American Bioproducts Co. · Sep 1995