Tracheostomy T-Tube

FDA 510(k) K930114 · Invotec International, Inc.

Substantially Equivalent

510(k) numberK930114

Submission

Device name
Tracheostomy T-Tube
Applicant
Invotec International, Inc.
Jacksonville, FL, US
Received
January 11, 1993
Decision date
March 19, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement 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

Other 510(k)s with product code BTR

510(k)DeviceApplicantDecision
K251794Tenax® Laser Resistant Endotracheal TubeBTR · Traditional Bryan Medical, Inc.09/03/2026SE
K253437Spiro-VISTABTR · Traditional Spiro Robotics06/12/2026SE
K250173Shiley™ Oral RAE Tracheal Tube Cuffless, Murphy Eye (113-XX) Shiley™ Nasal RAE Tracheal…BTR · Traditional Covidien, LLC10/06/2025SE
K243785Shiley™ Oral/Nasal Tracheal Tube with TaperGuard™ Cuff Reinforced, Murphy Eye Shiley™…BTR · Traditional Covidien, LLC09/25/2025SE
K243579AeroJet Ventilation CatheterBTR · Traditional Pipeline Medical Products, LLC08/13/2025SE
K251499Frova Intubating Introducer (C-CAE-14.0-70-FII); Frova Intubating Introducer…BTR · Special William Cook Europe Aps06/11/2025SE
K250243ProVu Single Use Video Stylet with Reinforced ET Tube (Size 6.5) (038-995-065U); ProVu…BTR · Traditional Flexicare Medical Limited.05/20/2025SE
K242495LMA Fastrach ETT SUBTR · Traditional Teleflex Medical04/29/2025SE
K241451Rusch Endotracheal Tubes (Reinforced); Rusch Endotracheal Tubes (Safety Clear); Rusch…BTR · Traditional Teleflex Incorporated02/11/2025SE
K233341Shiley™ Oral/Nasal Endotracheal Tube Intermediate Cuff, Non-DEHP (87430, 87435, 87440…BTR · Traditional Covidien, LLC05/20/2024SE

More from Covidien, LLC

510(k)DeviceDecision
K122040Invotec Laryngeal ElectrodeETN · Traditional 10/31/2013SE
K080740Clearview Endoscope CoverEOB · Traditional 12/31/2008SE
K030492Titanium Ossicular Replacment SystemETA · Traditional 03/03/2003SE
K973580Invotec Clean PadEFQ · Traditional 12/10/1997SE
K973578Invotec Ear Tampon (Wick) W/StringKCN · Traditional 11/06/1997SE
K971000Epistaxis Nasal PackEMX · Traditional 05/14/1997SE
K911041Invotec X-Ray Cassette Equipment DrapeIXA · Traditional 06/04/1991SE
K911040Invotec Microscope DrapeHMW · Traditional 06/03/1991SE
K911039Invotec Ear DrapeKKX · Traditional 05/13/1991SE
K901923Invotec Poly-Mesh Mandibular TrayJAZ · Traditional 10/31/1990SE

Questions and answers

When was Tracheostomy T-Tube cleared by the FDA?

Tracheostomy T-Tube (K930114) received a 510(k) decision of Substantially Equivalent on March 19, 1993, 67 days after the submission was received.

What is the product code of K930114?

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