Cleared Special

K073707 - GE DATEX-OHMEDA AISYS

K073707 is an FDA 510(k) clearance for GE DATEX-OHMEDA AISYS, 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 30-day FDA review.

K073707 · Datex-Ohmeda, Inc. · Anesthesiology device
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Jan 2008
Decision
30d
Days
Class 2
Risk

K073707 is an FDA 510(k) clearance for the GE DATEX-OHMEDA AISYS. 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 January 30, 2008 after a review of 30 days - a notably fast clearance cycle.

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. Low regulatory complexity profile. 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 - K073707

510(k) Number K073707 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 31, 2007
Decision Date January 30, 2008
Days to Decision 30 days
Submission Type Special
Review Panel Anesthesiology (AN)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
110d faster than avg
Panel avg: 140d · This submission: 30d
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 K073707.
COMPURECORD PERI-OPERATIVE ANESTHESIOLOGY INFORMATION SYSTEM
K083413 · Philips Medical Systems · Dec 2008
GE DATEX-OHMEDA AVANCE
K081844 · Datex-Ohmeda, Inc. · Aug 2008
NAVIGATOR APPLICATIONS SUITE
K081941 · GE Healthcare Finland Oy · Aug 2008
NAVIGATOR APPLICATIONS SUITE
K071097 · GE Healthcare Finland Oy · Oct 2007
GE DATEX-OHMEDA AVANCE ANESTHESIA SYSTEM
K071142 · Datex-Ohmeda · Jun 2007
GE DATEX-OHMEDA AISYS
K061609 · Datex-Ohmeda, Inc. · Jun 2006