Devilbiss Intellipap/ Sleepcube Bilevel St, DV56 St Series

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K093070 ↗

FDA Product Code

MNS

Device Class

Class II

Regulation

21 CFR Part 868.5895

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Devilbiss Intellipap Model Dv 5 Series

  Class II

  FDA 510(k) K071689 Active Cleared 7 Sep 2007

• Devilbiss Oxygen Cylinder Filling System 535 Series

  Class II

  FDA 510(k) K053240 Active Cleared 3 Feb 2006

• Quickie Interchange Fwd W/Lift Power Wheelchair

  Class II

  FDA 510(k) K043435 Active Cleared 11 Feb 2005

• Quickie Freestyle Power Wheelchair, Model G-424

  Class II

  FDA 510(k) K031289 Active Cleared 9 May 2003

• Power Recliner

  Class II

  FDA 510(k) K944423 Active Cleared 28 Nov 1994

• Quickie Rhapsody, Mwd Series II Power Wheelchair

  Class II

  FDA 510(k) K062701 Active Cleared 25 Sep 2006

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