Transtracheal Catheter (Acc. Ravussin).

FDA 510(k) K955461 · VBM Medizintechnik GmbH

Substantially Equivalent

510(k) numberK955461

Submission

Device name
Transtracheal Catheter (Acc. Ravussin).
Applicant
VBM Medizintechnik GmbH
Roy, UT, US
Received
November 29, 1995
Decision date
March 19, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
BTO – Tube, Tracheostomy (W/Wo Connector)
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5800
Specialty
Anesthesiology
Life-sustaining
Yes

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K2429215300600-5301000 Rota-Trach Disposable Standard Tracheostomy Tube, Cuffed, sizes…BTO · Traditional Vitaltec Corporation06/10/2025SE
K233713Pilling Tracheostomy TubesBTO · Traditional Teleflex Medical03/22/2024SE
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K173384BLUselect, non-fenestrated, BLUselect, non-fenestrated, cont, BLUselect, fenestrated…BTO · Traditional Smiths Medical Ads, Inc.04/10/2018SE
K120079Primed Tracheostomy Tubes (Multiple)BTO · Traditional Primed Halberstadt Medizintechnik GmbH05/24/2012SE
K101721Well Lead Tracheostomy Tube and Disposable Inner CannulaBTO · Special Regulatory and Marketing Services, Inc.03/24/2011SE
K100950Venner Pneux P.Y. (TM) Tracheostomy TubeBTO · Traditional Venner Medical (Singapore) Pte, Ltd.07/13/2010SE
K100480Rota-Trach Tracheostomy Tube Model Rota-TrachBTO · Traditional Vitaltec Corporation06/11/2010SE
K100283Versatube Tapered Tracheostomy Tube with Disposable Inner Cannula, Multiple, Prefixes…BTO · Traditional Cook, Inc.04/23/2010SE

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Questions and answers

When was Transtracheal Catheter (Acc. Ravussin). cleared by the FDA?

Transtracheal Catheter (Acc. Ravussin). (K955461) received a 510(k) decision of Substantially Equivalent on March 19, 1997, 476 days after the submission was received.

What is the product code of K955461?

The FDA product code is BTO – Tube, Tracheostomy (W/Wo Connector), a Class II (moderate risk) device regulated under 21 CFR 868.5800.