Cleared Traditional

K162140 - RemLogic

K162140 is an FDA 510(k) clearance for RemLogic, manufactured by Embla Systems. The device is a Class 2 Neurology device with product code OLZ cleared through the Traditional 510(k) pathway after a 122-day FDA review.

K162140 · Embla Systems · Neurology device
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Dec 2016
Decision
122d
Days
Class 2
Risk

K162140 is an FDA 510(k) clearance for the RemLogic. Classified as Automatic Event Detection Software For Polysomnograph With Electroencephalograph (product code OLZ), Class II - Special Controls.

Submitted by Embla Systems (Kanata, CA). The FDA issued a Cleared decision on December 1, 2016 after a review of 122 days - within the typical 510(k) review window.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.1400 - the FDA neurology 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 Neurology review framework, consistent with the majority of Class II 510(k) submissions.

View all Embla Systems devices

FDA 510(k) Submission Details - K162140

510(k) Number K162140 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 01, 2016
Decision Date December 01, 2016
Days to Decision 122 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
26d faster than avg
Panel avg: 148d · This submission: 122d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

OLZ Device Classification - Class 2, Special Controls

Product Code OLZ Automatic Event Detection Software For Polysomnograph With Electroencephalograph
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.1400
Definition Automatically Mark Electroencephalograph And Polysomongraph Signals In Order To Aid In Identification Of Such Events And Annotation Of Prolonged Psg Traces; Automatically Calculate Simple Measures Obtained From Recorded Signals (e.g. Magnitude, Time, Frequency And Simple Statistical Measures Of Marked Events); All Output Subject To Verification By Qualified User
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 Neurology devices follow this clearance model.

Regulatory Peers - OLZ Automatic Event Detection Software For Polysomnograph With Electroencephalograph

All 30
Devices cleared under the same product code (OLZ) and FDA review panel - the closest regulatory comparables to K162140.
NicoletOne
K173366 · Natus Neurology Incorporated · Jul 2018
REMbrandt
K163617 · Embla Systems · Apr 2017
EnsoSleep
K162627 · Ensodata, Inc. · Mar 2017
SANDMAN ELITE
K153353 · Embla Systems · Jun 2016
Sleep Profiler
K153412 · Advanced Brain Monitoring, Inc. · Mar 2016
Sleepware G3
K142988 · Respironics, Inc. · Mar 2015