The Visualized Endotracheal Tube System or Vett System
FDA 510(k) K973191 · Pulmonx
510(k) numberK973191
Submission
- Device name
- The Visualized Endotracheal Tube System or Vett System
- Applicant
- Pulmonx
Palo Alto, CA, US - Received
- August 25, 1997
- Decision date
- February 13, 1998
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
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) | Device | Applicant | Decision |
|---|---|---|---|
| K251794 | Tenax® Laser Resistant Endotracheal TubeBTR · Traditional | Bryan Medical, Inc. | 09/03/2026SE |
| K253437 | Spiro-VISTABTR · Traditional | Spiro Robotics | 06/12/2026SE |
| K250173 | Shiley Oral RAE Tracheal Tube Cuffless, Murphy Eye (113-XX) Shiley Nasal RAE Tracheal…BTR · Traditional | Covidien, LLC | 10/06/2025SE |
| K243785 | Shiley Oral/Nasal Tracheal Tube with TaperGuard Cuff Reinforced, Murphy Eye Shiley…BTR · Traditional | Covidien, LLC | 09/25/2025SE |
| K243579 | AeroJet Ventilation CatheterBTR · Traditional | Pipeline Medical Products, LLC | 08/13/2025SE |
| K251499 | Frova Intubating Introducer (C-CAE-14.0-70-FII); Frova Intubating Introducer…BTR · Special | William Cook Europe Aps | 06/11/2025SE |
| K250243 | ProVu Single Use Video Stylet with Reinforced ET Tube (Size 6.5) (038-995-065U); ProVu…BTR · Traditional | Flexicare Medical Limited. | 05/20/2025SE |
| K242495 | LMA Fastrach ETT SUBTR · Traditional | Teleflex Medical | 04/29/2025SE |
| K241451 | Rusch Endotracheal Tubes (Reinforced); Rusch Endotracheal Tubes (Safety Clear); Rusch…BTR · Traditional | Teleflex Incorporated | 02/11/2025SE |
| K233341 | Shiley Oral/Nasal Endotracheal Tube Intermediate Cuff, Non-DEHP (87430, 87435, 87440…BTR · Traditional | Covidien, LLC | 05/20/2024SE |
More from Covidien, LLC
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| K253096 | Chartis Precision CatheterCBI · Traditional | 02/13/2026SE |
| K222340 | Chartis Precision CatheterCBI · Traditional | 12/01/2022SE |
| K212494 | Lung Image AnalysisJAK · Traditional | 09/02/2021SE |
| K180011 | Pulmonx Chartis Tablet ConsoleBZG · Traditional | 07/13/2018SE |
| K111764 | Chartis ConsoleBZG · Special | 11/10/2011SE |
| K111522 | Chartis Catheter Model CHR-CA-12.0CBI · Special | 09/29/2011SE |
| K083883 | Chartis CatheterCBI · Traditional | 06/25/2009SE |
| K083199 | Chartis ConsoleBZG · Traditional | 06/25/2009SE |
Questions and answers
When was The Visualized Endotracheal Tube System or Vett System cleared by the FDA?
The Visualized Endotracheal Tube System or Vett System (K973191) received a 510(k) decision of Substantially Equivalent on February 13, 1998, 172 days after the submission was received.
What is the product code of K973191?
The FDA product code is BTR – Tube, Tracheal (W/Wo Connector), a Class II (moderate risk) device regulated under 21 CFR 868.5730.