Rehabilitation Tables

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K854947 ↗

FDA Product Code

INQ

Device Class

Class I

Regulation

21 CFR Part 890.3760

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

• Rotagym

  Class II

  FDA 510(k) K832940 Active Cleared 7 Nov 1983

• Accutrac Traction Unit

  Class II

  FDA 510(k) K930691 Active Cleared 22 Jul 1993

• Adjustable Treatment Tables

  Not classified

  FDA 510(k) K851690 Active Cleared 7 May 1985

• Latham Table

  Class I

  FDA 510(k) K930692 Active Cleared 2 Feb 1994

• Physical Medicine & Rehabilitation Equip

  Class I

  FDA 510(k) K822906 Active Cleared 15 Oct 1982

• Medtron Type P-300 Ultrasonic Therapy Unit

  Class II

  FDA 510(k) K861864 Active Cleared 14 Jul 1986

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