Lic-Orthion Multi-Therapy Treatment Table

No FDA recalls found in the data synced 9 Oct 2026.

510(k) Number

K862022 ↗

FDA Product Code

JFB

Device Class

Class II

Regulation

21 CFR Part 890.5880

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

• Sesam Treatment Table

  Class I

  FDA 510(k) K830855 Active Cleared 5 Apr 1983

• Ob Tilt

  Class I

  FDA 510(k) K830849 Active Cleared 5 Apr 1983

• Daisy (Absorbent Incontinence Shield)

  Class I

  FDA 510(k) K854730 Active Cleared 6 Feb 1986

• Anatom System

  Class I

  FDA 510(k) K843233 Active Cleared 25 Oct 1984

• Patient Examination Gloves (Latex)

  Class I

  FDA 510(k) K891649 Active Cleared 4 Apr 1989

• Bath Tub Seat & Bath Board

  Class I

  FDA 510(k) K830851 Active Cleared 5 Apr 1983

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