Appollo Bath

No FDA recalls on record, checked 11 Oct 2026.

510(k) Number

K882669 ↗

FDA Product Code

ILK

FDA applicant

Electric Mobility, LLC

Device Class

Class II

Regulation

21 CFR Part 890.5150

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

• Electric Mobility Rascal

  Class II

  FDA 510(k) K924515 Active Cleared 28 Mar 1994

• Rascal Power Chair

  Class II

  FDA 510(k) K972370 Active Cleared 14 Nov 1997

• Cavalier Scooters

  Class II

  FDA 510(k) K991281 Active Cleared 27 Oct 1999

• Electric Mobility's Sparky

  Class II

  FDA 510(k) K874739 Active Cleared 22 Apr 1988

• Electric Mobility Rascal and Chauffer Scooters

  Class II

  FDA 510(k) K002616 Active Cleared 11 Dec 2000

• Xlt, Rea Comfort, Spirea, Zoom

  Class I

  FDA 510(k) K943936 Active Cleared 21 Sep 1994

See all devices from Electric Mobility Corp. →