Cleared Traditional

K041662 - APNEA RISK EVALUATION SYSTEM (ARES)

K041662 is an FDA 510(k) clearance for APNEA RISK EVALUATION SYSTEM (ARES), manufactured by Advanced Brain Monitoring, Inc.. The device is a Class 2 Anesthesiology device with product code MNR cleared through the Traditional 510(k) pathway after a 118-day FDA review.

K041662 · Advanced Brain Monitoring, Inc. · Anesthesiology device
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Oct 2004
Decision
118d
Days
Class 2
Risk

K041662 is an FDA 510(k) clearance for the APNEA RISK EVALUATION SYSTEM (ARES). Classified as Ventilatory Effort Recorder (product code MNR), Class II - Special Controls.

Submitted by Advanced Brain Monitoring, Inc. (Carlsbad, US). The FDA issued a Cleared decision on October 14, 2004 after a review of 118 days - within the typical 510(k) review window.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.2375 - the FDA anesthesiology and respiratory 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 Anesthesiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Advanced Brain Monitoring, Inc. devices

FDA 510(k) Submission Details - K041662

510(k) Number K041662 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 18, 2004
Decision Date October 14, 2004
Days to Decision 118 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
22d faster than avg
Panel avg: 140d · This submission: 118d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MNR Device Classification - Class 2, Special Controls

Product Code MNR Ventilatory Effort Recorder
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.2375
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 Anesthesiology devices follow this clearance model.

Regulatory Peers - MNR Ventilatory Effort Recorder

All 65
Devices cleared under the same product code (MNR) and FDA review panel - the closest regulatory comparables to K041662.
CADWELL EASYNET NASAL PRESSURE MODULE
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K051313 · Salter Labs · Sep 2005
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K021845 · Respironics, Inc. · May 2004
APNOESCREEN PRO, ALPHA SCREEN PRO
K000396 · Erich Jaeger, Inc. · Dec 2000
SUZANNE
K990565 · Nellcor Puritan Bennett, Inc. · Aug 1999