Shiley Extended Length, Disposable Cannula, Tracheostomy Tube: Cuffed, Distal Extension, Cuffed, Proximal Extension, Cuf

FDA 510(k) K971267 · Mallinckrodt Medical

Substantially Equivalent

510(k) numberK971267

Submission

Device name
Shiley Extended Length, Disposable Cannula, Tracheostomy Tube: Cuffed, Distal Extension, Cuffed, Proximal Extension, Cuf
Applicant
Mallinckrodt Medical
St Louis, MO, US
Received
April 4, 1997
Decision date
September 25, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

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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More from Smiths Medical Asd, Inc.

510(k)DeviceDecision
K082520Sealguard Evac Endotracheal and Endotracheal TubesBTR · Special 10/02/2008SE
K051416Shiley Tracheosoft XLT Extended Length Tracheostomy Tube and Inner CannulaJOH · Special 06/16/2005SE
K972258Hi-Care Closed Suction SystemBSY · Traditional 12/29/1997SE
K963732Percutaneous Dual Cannula Tracheostomy Tube with Low Pressure/Low Profile Cuff and…JOH · Traditional 06/26/1997SE
K955721Cuffed Oropharyngeal Airway (Copa)CAE · Traditional 03/28/1997SE
K965132Hi-Lo Evac and Evac II Endotracheal TubesBTR · Traditional 03/20/1997SE
K962045Anesthesia Breathing Circuit/Anesthesia Breathing KitCAH · Traditional 11/26/1996SE
K962173Shikey Tracheostomy Tubes and AccessoriesJOH · Traditional 10/04/1996SE
K955680Shiley Cuffed Pediatric Tracheostomy Tube; Long CuffedJOH · Traditional 03/13/1996SE
K954749Mallinckrodt Shiley 15MM CapJOH · Traditional 01/24/1996SE

Questions and answers

When was Shiley Extended Length, Disposable Cannula, Tracheostomy Tube: Cuffed, Distal Extension, Cuffed, Proximal Extension, Cuf cleared by the FDA?

Shiley Extended Length, Disposable Cannula, Tracheostomy Tube: Cuffed, Distal Extension, Cuffed, Proximal Extension, Cuf (K971267) received a 510(k) decision of Substantially Equivalent on September 25, 1997, 174 days after the submission was received.

What is the product code of K971267?

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