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

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K971267 ↗

FDA Product Code

JOH

Device Class

Class II

Regulation

21 CFR Part 868.5800

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Percutaneous Transluminal Angioplasty Catheter

  Class II

  FDA 510(k) K905773 Active Cleared 30 Jan 1991

• Softouch Guiding Catheter

  Class II

  FDA 510(k) K905547 Active Cleared 5 Feb 1991

• Mallard Medical Model 2400 Anesthesia Ventilator

  Class II

  FDA 510(k) K902405 Active Cleared 4 Mar 1991

• Hygrobac, S Hygroboy and Hygrobaby Open recall

  Class II

  FDA 510(k) K941381 Active Cleared 15 Apr 1994

• Softtouch(R) Guiding Catheter

  Class II

  FDA 510(k) K912199 Active Cleared 30 Jul 1991

• Sealguard Evac Endotracheal and Endotracheal Tubes

  Class II

  FDA 510(k) K082520 Active Cleared 2 Oct 2008

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