Cleared Traditional

K932566 - AGGRO/LINK CONTROL SOFTWARE

K932566 is an FDA 510(k) clearance for AGGRO/LINK CONTROL SOFTWARE, manufactured by Chrono-Log Corp.. The device is a Class 2 Hematology device with product code JBX cleared through the Traditional 510(k) pathway after a 159-day FDA review.

K932566 · Chrono-Log Corp. · Hematology device
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Nov 1993
Decision
159d
Days
Class 2
Risk

K932566 is an FDA 510(k) clearance for the AGGRO/LINK CONTROL SOFTWARE. Classified as Aggregrometer, Platelet (product code JBX), Class II - Special Controls.

Submitted by Chrono-Log Corp. (Havertown, US). The FDA issued a Cleared decision on November 2, 1993 after a review of 159 days - an extended review cycle.

This device falls under the Hematology FDA review panel, regulated under 21 CFR 864.6675 - 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.

View all Chrono-Log Corp. devices

FDA 510(k) Submission Details - K932566

510(k) Number K932566 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 27, 1993
Decision Date November 02, 1993
Days to Decision 159 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
46d slower than avg
Panel avg: 113d · This submission: 159d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JBX Device Classification - Class 2, Special Controls

Product Code JBX Aggregrometer, Platelet
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 864.6675
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 - JBX Aggregrometer, Platelet

Devices cleared under the same product code (JBX) and FDA review panel - the closest regulatory comparables to K932566.
ARACHIDONIC ACID
K912774 · Helena Laboratories · Aug 1991
PAT PLATELET AGGREGATION TEST
K881829 · Streck Laboratories, Inc. · Jul 1988
ASSERACHROM B-TG KIT
K862775 · American Bioproducts Co. · Oct 1986
RISTOCETIN PLATELET AGGREGA-REAGENT TEST
K832929 · Sigma Chemical Co. · Sep 1983
PLATELET AGGREGATION PROFILER #PAP-4
K821005 · Bio/Data Corp. · Jun 1982
ARACHIDONIC ACID
K811290 · Bio/Data Corp. · Jul 1981