Disposable Uncuffed Endotracheal Tube

FDA 510(k) K925855 · Coast Medical Corp.

Substantially Equivalent

510(k) numberK925855

Submission

Device name
Disposable Uncuffed Endotracheal Tube
Applicant
Coast Medical Corp.
Orange, CA, US
Received
November 17, 1992
Decision date
February 18, 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

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More from Covidien, LLC

510(k)DeviceDecision
K952243Extension Set/I.V. SetFPK · Traditional 07/26/1995SE
K930929Esophageal StethoscopeBZT · Traditional 03/17/1995SE
K944729Stylet Sheath with Locking Cap and Reusable Battery Operated Light SourceBSR · Traditional 12/21/1994SE
K943270Surface Temperature ProbesFLL · Traditional 12/05/1994SE
K943495Disposable Esophageal StethoscopeBZT · Traditional 09/08/1994SE
K943110Gas Sampling InterfacesBYX · Traditional 08/19/1994SE
K930930Coast Medical, Inc. Rectal ProbeFLL · Traditional 02/25/1994SE
K925781Disposable Cuffed Endotracheal TubeBTR · Traditional 04/19/1993SE
K921077Disposable Intubation KitsBTR · Traditional 08/25/1992SE
K921353Nasopharyngeal AirwayBTQ · Traditional 06/11/1992SE

Questions and answers

When was Disposable Uncuffed Endotracheal Tube cleared by the FDA?

Disposable Uncuffed Endotracheal Tube (K925855) received a 510(k) decision of Substantially Equivalent on February 18, 1993, 93 days after the submission was received.

What is the product code of K925855?

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