Cleared Traditional

K003707 - CARDIONET AMBULATORY ECG MONITOR, MODEL CN1000A

K003707 is an FDA 510(k) clearance for CARDIONET AMBULATORY ECG MONITOR, manufactured by Cardionet. The device is a Class 2 Cardiovascular device with product code MWJ cleared through the Traditional 510(k) pathway after a 166-day FDA review.

K003707 · Cardionet · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 2001
Decision
166d
Days
Class 2
Risk

K003707 is an FDA 510(k) clearance for the CARDIONET AMBULATORY ECG MONITOR, MODEL CN1000A. Classified as Electrocardiograph, Ambulatory (without Analysis) (product code MWJ), Class II - Special Controls.

Submitted by Cardionet (San Diego, US). The FDA issued a Cleared decision on May 16, 2001 after a review of 166 days - an extended review cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2800 - the FDA cardiovascular device oversight 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 Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

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FDA 510(k) Submission Details - K003707

510(k) Number K003707 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 01, 2000
Decision Date May 16, 2001
Days to Decision 166 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
41d slower than avg
Panel avg: 125d · This submission: 166d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MWJ Device Classification - Class 2, Special Controls

Product Code MWJ Electrocardiograph, Ambulatory (without Analysis)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2800
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 - MWJ Electrocardiograph, Ambulatory (without Analysis)

All 34
Devices cleared under the same product code (MWJ) and FDA review panel - the closest regulatory comparables to K003707.
SPIDERVIEW
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K992584 · Nhe Corp. · Jan 2000
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K993643 · Nexan Telemed , Ltd. · Dec 1999
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K993617 · Braemar Corp. · Nov 1999