Concept Endotracheal Tube

FDA 510(k) K801213 · Concept, Inc.

Substantially Equivalent

510(k) numberK801213

Submission

Device name
Concept Endotracheal Tube
Applicant
Concept, Inc.
Mchenry, IL, US
Received
May 20, 1980
Decision date
May 28, 1980
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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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
K912640Concept Endosteal Fixation DeviceHWC · Traditional 05/01/1992SE
K912957Concept MicromillHRX · Traditional 10/04/1991SE
K896648Concept Unicompartmental Knee SystemHSX · Traditional 06/05/1990SN
K894929Staple Fixation SystemJDR · Traditional 08/30/1989SE
K892376Intravision(Tm) Arthroscope System (Add'L Appli.)HRX · Traditional 08/01/1989SE
K891109Panda(R) Needle Catheter Jejunostomy TubeKNT · Traditional 05/08/1989SE
K881954Concept Power SystemHSZ · Traditional 11/09/1988SE
K884255Concept CCT-5200, Thermal Therapy SystemILO · Traditional 11/08/1988SE
K882121C-Flo Suction TubeDXQ · Traditional 06/20/1988SE
K880414Tendon HarvesterHRX · Traditional 03/25/1988SE

Questions and answers

When was Concept Endotracheal Tube cleared by the FDA?

Concept Endotracheal Tube (K801213) received a 510(k) decision of Substantially Equivalent on May 28, 1980, 8 days after the submission was received.

What is the product code of K801213?

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