Lazer-Trach Tracheal Tube

FDA 510(k) K922894 · Sheridan Catheter Corp.

Substantially Equivalent

510(k) numberK922894

Submission

Device name
Lazer-Trach Tracheal Tube
Applicant
Sheridan Catheter Corp.
Argyle, NY, US
Received
June 16, 1992
Decision date
May 7, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary 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
K897046Laser Resistant Tracheal TubeCBI · Traditional 03/23/1990SE
K890823Accessory to Clinical Electronic ThermometerFLL · Traditional 05/05/1989SE
K884765Clinical Electronic ThermometersFLL · Traditional 02/16/1989SE
K882918Kim Naso-Intestinal TubeKNT · Traditional 12/05/1988SE
K882127Clinical Electronic ThermometersFLL · Traditional 08/04/1988SE
K881368Clinical Electonic ThermometersFLL · Traditional 07/13/1988SE
K881293Sheridan Electrosurgery Protection FilterBZT · Traditional 06/16/1988SE
K881873Introduction/Drainage Catheter & AccessGBS · Traditional 05/18/1988SE
K880960Ndyag Laser Tracheal TubeBTR · Traditional 04/29/1988SE
K875226Esophageal Obturator/Tracheal TubeCAO · Traditional 01/19/1988SE

Questions and answers

When was Lazer-Trach Tracheal Tube cleared by the FDA?

Lazer-Trach Tracheal Tube (K922894) received a 510(k) decision of Substantially Equivalent on May 7, 1993, 325 days after the submission was received.

What is the product code of K922894?

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