Cleared Special

K123125 - GE DATEX-OHMEDA AVANCE CS2

K123125 is an FDA 510(k) clearance for GE DATEX-OHMEDA AVANCE CS2, manufactured by Datex-Ohmeda, Inc.. The device is a Class 2 Anesthesiology device with product code BSZ cleared through the Special 510(k) pathway after a 125-day FDA review.

K123125 · Datex-Ohmeda, Inc. · Anesthesiology device
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Feb 2013
Decision
125d
Days
Class 2
Risk

K123125 is an FDA 510(k) clearance for the GE DATEX-OHMEDA AVANCE CS2. Classified as Gas-machine, Anesthesia (product code BSZ), Class II - Special Controls.

Submitted by Datex-Ohmeda, Inc. (Madison, US). The FDA issued a Cleared decision on February 6, 2013 after a review of 125 days - within the typical 510(k) review window.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5160 - the FDA anesthesiology and respiratory device framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Standard predicate reliance. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Datex-Ohmeda, Inc. devices

FDA 510(k) Submission Details - K123125

510(k) Number K123125 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 04, 2012
Decision Date February 06, 2013
Days to Decision 125 days
Submission Type Special
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
15d faster than avg
Panel avg: 140d · This submission: 125d
Pathway characteristics
Modification to existing cleared device.

BSZ Device Classification - Class 2, Special Controls

Product Code BSZ Gas-machine, Anesthesia
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5160
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 - BSZ Gas-machine, Anesthesia

All 110
Devices cleared under the same product code (BSZ) and FDA review panel - the closest regulatory comparables to K123125.
A7 Anesthesia System
K142552 · Shenzhen Mindray Bio-Medical Electronics Co., Ltd. · Jan 2015
GE DATEX-OHMEDA AISYS CS2 (AISYS CS^2)
K132530 · Datex-Ohmeda, Inc. · Dec 2013
GE DATEX-OHMEDA AVANCE CS2
K131945 · Datex-Ohmeda · Aug 2013
AESPIRE 7900, AESPIRE VIEW
K122445 · Datex-Ohmeda · Oct 2012
GE DATEX-OHMEDA AVANCE
K112722 · Datex-Ohmeda, Inc. · Dec 2011
GE DATEX-OHMEDA AISYS
K110213 · Datex-Ohmeda, Inc. · Jul 2011