Cleared Special

K110930 - ACTIVE WASTE GAS SCAVENGER

K110930 is an FDA 510(k) clearance for ACTIVE WASTE GAS SCAVENGER, manufactured by G. Dundas Co.,Inc.. The device is a Class 2 Anesthesiology device with product code CBN cleared through the Special 510(k) pathway after a 80-day FDA review.

K110930 · G. Dundas Co.,Inc. · Anesthesiology device
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Jun 2011
Decision
80d
Days
Class 2
Risk

K110930 is an FDA 510(k) clearance for the ACTIVE WASTE GAS SCAVENGER. Classified as Apparatus, Gas-scavenging (product code CBN), Class II - Special Controls.

Submitted by G. Dundas Co.,Inc. (Black Diamond, US). The FDA issued a Cleared decision on June 23, 2011 after a review of 80 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5430 - 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 G. Dundas Co.,Inc. devices

FDA 510(k) Submission Details - K110930

510(k) Number K110930 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 04, 2011
Decision Date June 23, 2011
Days to Decision 80 days
Submission Type Special
Review Panel Anesthesiology (AN)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
60d faster than avg
Panel avg: 140d · This submission: 80d
Pathway characteristics
Modification to existing cleared device.

CBN Device Classification - Class 2, Special Controls

Product Code CBN Apparatus, Gas-scavenging
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5430
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 - CBN Apparatus, Gas-scavenging

All 14
Devices cleared under the same product code (CBN) and FDA review panel - the closest regulatory comparables to K110930.
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