Cleared Abbreviated

K152701 - Matrix Mini ECG Monitor

K152701 is the FDA 510(k) clearance for Matrix Mini ECG Monitor by Global Instrumentation, LLC. It is a Class 2 Cardiovascular device (product code DSI) cleared through the Abbreviated 510(k) pathway after a 214-day FDA review.

K152701 · Global Instrumentation, LLC · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 2016
Decision
214d
Days
Class 2
Risk

K152701 is an FDA 510(k) clearance for the Matrix Mini ECG Monitor. Classified as Detector And Alarm, Arrhythmia (product code DSI), Class II - Special Controls.

Submitted by Global Instrumentation, LLC (Manlius, US). The FDA issued a Cleared decision on April 22, 2016 after a review of 214 days - an extended review cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1025 - the FDA cardiovascular device oversight framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Global Instrumentation, LLC devices

Submission Details

510(k) Number K152701 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 21, 2015
Decision Date April 22, 2016
Days to Decision 214 days
Submission Type Abbreviated
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
89d slower than avg
Panel avg: 125d · This submission: 214d
Pathway characteristics
Standards-based clearance path.

Device Classification

Product Code DSI Detector And Alarm, Arrhythmia
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1025
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 Cardiovascular devices follow this clearance model.

Regulatory Peers - DSI Detector And Alarm, Arrhythmia

All 212
Devices cleared under the same product code (DSI) and FDA review panel - the closest regulatory comparables to K152701.
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IntelliVue Patient Monitor
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Medtronic Patient Asistant
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IntelliVue Patient Monitor
K150310 · Philips Medizin Systeme Boeblingen GmbH · May 2015