Chump

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

510(k) Number

K030017 ↗

FDA Product Code

IOR

Device Class

Class I

Regulation

21 CFR Part 890.3850

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

• Mechanical Wheelchair - Boing

  Class I

  FDA 510(k) K945534 Active Cleared 2 Jan 1995

• Mechanical Wheelchair- Impact

  Class I

  FDA 510(k) K945152 Active Cleared 1 May 1995

• Mechanical Wheelchair - Supernova

  Class I

  FDA 510(k) K945533 Active Cleared 2 Jan 1995

• Mechanical Wheelchair- Avenger

  Class I

  FDA 510(k) K945148 Active Cleared 12 May 1995

• Spazz

  Class I

  FDA 510(k) K010823 Active Cleared 27 Apr 2001

• Mechanical Wheerchair- Eclipse

  Class I

  FDA 510(k) K945150 Active Cleared 12 May 1995

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