Patient Guided Knee Exerciser

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K820120 ↗

FDA Product Code

BXB

Device Class

Class I

Regulation

21 CFR Part 890.5380

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

• Plug-Lok Cement Restirctor

  Class II

  FDA 510(k) K791125 Active Cleared 27 Jun 1979

• Spectron Primary Stem Femoral Prosthes

  Class II

  FDA 510(k) K823727 Active Cleared 8 Mar 1983

• Reuter Bobbin Ventila. Tube-Titanium

  Class II

  FDA 510(k) K820362 Active Cleared 2 Mar 1982

• Pullen Plastic-Pore Plugs

  Class II

  FDA 510(k) K772066 Active Cleared 20 Dec 1977

• Spoon-Bobbin Drain Tube W/ Wire, Otology

  Class II

  FDA 510(k) K760438 Active Cleared 21 Sep 1976

• Colles Fracture Frame

  Class II

  FDA 510(k) K830154 Active Cleared 2 Feb 1983

See all devices from Richard'S Medical Equip., Inc. →