Cleared Traditional

K260907 - BIS™ Advance pEEG Module

K260907 is an FDA 510(k) clearance for BIS Advance pEEG Module, manufactured by Covidien LP. The device is a Class 2 Anesthesiology device with product code OLW cleared through the Traditional 510(k) pathway after a 147-day FDA review.

K260907 · Covidien LP · Anesthesiology device
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Aug 2026
Decision
147d
Days
Class 2
Risk

K260907 is an FDA 510(k) clearance for the BIS™ Advance pEEG Module. Classified as Index-generating Electroencephalograph Software (product code OLW), Class II - Special Controls.

Submitted by Covidien LP (Mansfield, US). The FDA issued a Cleared decision on August 13, 2026 after a review of 147 days - within the typical 510(k) review window.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 882.1400 - 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 Covidien LP devices

FDA 510(k) Submission Details - K260907

510(k) Number K260907 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 19, 2026
Decision Date August 13, 2026
Days to Decision 147 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
7d slower than avg
Panel avg: 140d · This submission: 147d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

OLW Device Classification - Class 2, Special Controls

Product Code OLW Index-generating Electroencephalograph Software
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.1400
Definition Analyze Electrical Activity Of The Brain By Transformation Of Electroencephalograph Signals Into A Dimensionless Index Number For Use And Interpretation By A 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 Anesthesiology devices follow this clearance model.

Regulatory Peers - OLW Index-generating Electroencephalograph Software

All 35
Devices cleared under the same product code (OLW) and FDA review panel - the closest regulatory comparables to K260907.
SedLine Sedation Monitor
K260880 · Masimo Corporation · Jul 2026
BIS™ Advance Monitoring System
K230693 · Covidien, LLC · Feb 2024
Brain Anesthesia Response Monitor (Bar Monitor)
K213273 · Cortical Dynamics , Ltd. · Sep 2023
Masimo SedLine Sedation Monitor and Accessories
K203113 · Masimo Corporation · Feb 2022
NeuroSENSE Monitoring System, Model NS-901
K202621 · Neurowave Systems, Inc. · Aug 2021
SedLine Sedation Monitor
K172890 · Masimo Corporation · Jan 2018