Quadraplegic Walking Aid

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K772267 ↗

FDA Product Code

IPS

Device Class

Class I

Regulation

21 CFR Part 890.3075

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

• Instrument Tray

  Class I

  FDA 510(k) K772266 Active Cleared 20 Jan 1978

• Three Way Infusion Set

  Class II

  FDA 510(k) K841882 Active Cleared 5 Jun 1984

• Iv Filter Extension Set

  Class II

  FDA 510(k) K860803 Active Cleared 9 Apr 1986

• Trapeze Bar Knocked Down

  Class I

  FDA 510(k) K772262 Active Cleared 26 Jan 1978

• Setup Walker Over Toilet Construc.

  Class I

  FDA 510(k) K772270 Active Cleared 20 Dec 1977

• Ambulatory Infusion Pump Drug Reservoir

  Class II

  FDA 510(k) K870524 Active Cleared 6 May 1987

See all devices from Med Fusion Systems, Inc. →