Xomed Treace Jet Ventilation Tube

FDA 510(k) K922880 · Xomed-Treace, Inc.

Substantially Equivalent

510(k) numberK922880

Submission

Device name
Xomed Treace Jet Ventilation Tube
Applicant
Xomed-Treace, Inc.
Jacksonville, FL, US
Received
June 15, 1992
Decision date
April 15, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
BTR – Tube, Tracheal (W/Wo Connector)
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5730
Specialty
Anesthesiology
Life-sustaining
Yes

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More from Covidien, LLC

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K932771Battery Powered, Disposable Endoscope Light SourceEQH · Traditional 08/24/1994SE
K933672Xomed-Treace ScopesheathEOB · Traditional 07/18/1994SE
K934426Nerve Integrity MONITOR-2 (NIM-2 XL)ETN · Traditional 05/13/1994SE
K933105Xomed-Treace Rigid Rod Lens EndoscopeEOB · Traditional 01/05/1994SE
K925640Xomed-Treace Emg Endotracheal TubeenETN · Traditional 08/17/1993SE
K923830Xomed-Treace AlphascopeERA · Traditional 11/09/1992SE
K912753Xomed-Treace Positrol Footpedal Suction ControlGCX · Traditional 09/23/1991SE

Questions and answers

When was Xomed Treace Jet Ventilation Tube cleared by the FDA?

Xomed Treace Jet Ventilation Tube (K922880) received a 510(k) decision of Substantially Equivalent on April 15, 1993, 304 days after the submission was received.

What is the product code of K922880?

The FDA product code is BTR – Tube, Tracheal (W/Wo Connector), a Class II (moderate risk) device regulated under 21 CFR 868.5730.