MLT Tube Microlaryngeal Tracheal Tube)

FDA 510(k) K801005 · National Catheter Co. Div. Mallinckrodt

Substantially Equivalent

510(k) numberK801005

Submission

Device name
MLT Tube Microlaryngeal Tracheal Tube)
Applicant
National Catheter Co. Div. Mallinckrodt
Mchenry, IL, US
Received
April 28, 1980
Decision date
May 23, 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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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
K802918Anthron Catheter SetFOZ · Traditional 04/21/1981SE
K802505Double Lumen Tracheal TubeBTR · Traditional 03/13/1981SE
K810321Reinforced Tracheostomy Tube Set(Tentat)BTO · Traditional 03/04/1981SE
K801924Hi-Lo Temp Gen. Purpose Temp. ProbeFLL · Traditional 09/09/1980SE
K791190Stethoscope with Temperature SensorBZT · Traditional 07/06/1979SE
K781665Tube, Leatherman/ImbruceGBA · Traditional 12/15/1978SE
K770727Manipulator & Injector, UterineKNA · Traditional 04/26/1977SE

Questions and answers

When was MLT Tube Microlaryngeal Tracheal Tube) cleared by the FDA?

MLT Tube Microlaryngeal Tracheal Tube) (K801005) received a 510(k) decision of Substantially Equivalent on May 23, 1980, 25 days after the submission was received.

What is the product code of K801005?

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