Shiley Specialized Tracheostomy Tube

FDA 510(k) K903435 · Shiley, Inc.

Substantially Equivalent

510(k) numberK903435

Submission

Device name
Shiley Specialized Tracheostomy Tube
Applicant
Shiley, Inc.
Irvine, CA, US
Received
July 31, 1990
Decision date
October 2, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JOH – Tube Tracheostomy And Tube Cuff
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5800
Specialty
Anesthesiology
Life-sustaining
Yes

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K172720TRACOE silcosoft Tracheostomy TubeJOH · Traditional Tracoe Medical GmbH04/27/2018SE
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More from Smiths Medical Asd, Inc.

510(k)DeviceDecision
K920594Shiley Perfusion Tubing SetsDTM · Traditional 03/18/1993SE
K910991Shiley Therapeutic Autotransfusion SystemCAC · Traditional 11/27/1991SE
K911876Shiley Plexus(R) Venous Reservoir, PVR1200DTN · Traditional 08/09/1991SE
K910923BCD AdvancedDTR · Traditional 04/09/1991SE
K901548Biomedical Sensors-Shiley BGM 4000 Intra Blood GasCCC · Traditional 01/14/1991SE
K901624Shiley Plexus Integral Reservoir Hollow Fiber Oxy.DTZ · Traditional 07/03/1990SE
K901250Plexus 2(TM) Infant Hollow Fiber OxygenatorDTZ · Traditional 06/11/1990SE
K901249Plexus 3.5(TM) Pediatric Hollow Fiber OxygenatorDTZ · Traditional 06/11/1990SE
K900797Stockert Shiley Dual Pressure Control Module XRDXS · Traditional 05/10/1990SE
K900548Shiley Phonation ValveBTO · Traditional 04/23/1990SE

Questions and answers

When was Shiley Specialized Tracheostomy Tube cleared by the FDA?

Shiley Specialized Tracheostomy Tube (K903435) received a 510(k) decision of Substantially Equivalent on October 2, 1990, 63 days after the submission was received.

What is the product code of K903435?

The FDA product code is JOH – Tube Tracheostomy And Tube Cuff, a Class II (moderate risk) device regulated under 21 CFR 868.5800.