Quickie P100 Series, Quickie P200 Series, Quickie P300 Series, Models P100, P110, P120, P190, P190R, P500, P200, P210, P320, P300

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

510(k) Number

K981462 ↗

FDA Product Code

ITI

Models / Variants

P100

P110

P120

P190

P190R

P500

P200

P210

P320

P300

Device Class

Class II

Regulation

21 CFR Part 890.3860

Advisory Committee

Physical Medicine

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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