BLUselect, non-fenestrated, BLUselect, non-fenestrated, cont, BLUselect, fenestrated, BLUselect Suctionaid, BLUpere Dilation Trachestomy Kit, without tube

FDA 510(k) K173384 · Smiths Medical Ads, Inc.

Substantially Equivalent

510(k) numberK173384

Submission

Device name
BLUselect, non-fenestrated, BLUselect, non-fenestrated, cont, BLUselect, fenestrated, BLUselect Suctionaid, BLUpere Dilation Trachestomy Kit, without tube
Applicant
Smiths Medical Ads, Inc.
Plymouth, MN, US
Received
October 30, 2017
Decision date
April 10, 2018
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary 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

Other 510(k)s with product code BTO

510(k)DeviceApplicantDecision
K253063Venti-Trach Tracheostomy Tube (570 Series); Venti-Trach Tracheostomy Tube (571 Series)…BTO · Special Vitaltec Corporation09/11/2026SE
K2429215300600-5301000 Rota-Trach Disposable Standard Tracheostomy Tube, Cuffed, sizes…BTO · Traditional Vitaltec Corporation06/10/2025SE
K233713Pilling Tracheostomy TubesBTO · Traditional Teleflex Medical03/22/2024SE
K192511Venner PneuX™ TT (Tracheostomy Tube) Size 7.0 mm, Venner PneuX™ TT (Tracheostomy Tube)…BTO · Traditional Venner Medical (Singapore) Pte, Ltd.07/22/2020SE
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
K083031Portex Uniperc Percutaneous Dilation Tracheostomy KitBTO · Traditional Smiths Medical Asd, Inc.08/18/2009SE

More from Smiths Medical Asd, Inc.

510(k)DeviceDecision
K170982CADD®- Solis Ambulatory Infusion Pump with Wireless Communication; CADD®-Solis Infusion…MEA · Traditional 08/24/2017SE

Questions and answers

When was BLUselect, non-fenestrated, BLUselect, non-fenestrated, cont, BLUselect, fenestrated, BLUselect Suctionaid, BLUpere Dilation Trachestomy Kit, without tube cleared by the FDA?

BLUselect, non-fenestrated, BLUselect, non-fenestrated, cont, BLUselect, fenestrated, BLUselect Suctionaid, BLUpere Dilation Trachestomy Kit, without tube (K173384) received a 510(k) decision of Substantially Equivalent on April 10, 2018, 162 days after the submission was received.

What is the product code of K173384?

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