Portex BLUxl Extra Length Tracheostomy Tube, BLUxl Suctionaid Extra Length Tracheostomy Tube, BLUxl Extra Length Tracheostomy Inner Cannula

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

510(k) Number

K210833 ↗

FDA Product Code

JOH

Device Class

Class II

Regulation

21 CFR Part 868.5800

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Level 1 Snuggle Warm Pediatric and Large Pediatric Underbody Blanket

  Class II

  FDA 510(k) K061513 Active Cleared 1 Aug 2006

• SAF-T Closed Blood Collection System with SAF-Holder Device, Model 99200

  Class II

  FDA 510(k) K072783 Active Cleared 30 Nov 2007

• Thera-Heat Heated Humidifier and Adult Dual and Single Limb Heated Wire Ventilator Breathing Circuits

  Class II

  FDA 510(k) K071958 Active Cleared 21 Nov 2007

• Port-A-Cath Power P.A.C. Implantable Venous Access Systems

  Class II

  FDA 510(k) K093414 Active Cleared 1 Mar 2010

• Thera- Heat Heated Humidifier, Model RC70000, RC70072, RC70075, RC70077, RC70012

  Class II

  FDA 510(k) K092256 Active Cleared 20 Oct 2010

• EchoGlo Needle

  Class II

  FDA 510(k) K171968 Active Cleared 25 Jan 2018

See all devices from Smiths Medical Asd, Inc. →