Thermo Shortwave Diathermy

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K852166 ↗

FDA Product Code

IMJ

Device Class

Class II

Regulation

21 CFR Part 890.5290

Advisory Committee

Physical Medicine

FDA Decision

SN

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  Class II

  FDA 510(k) K960969 Active Cleared 15 May 1996

• VACO Suction Electrode Unit

  Class II

  FDA 510(k) K860758 Active Cleared 2 May 1986

• CARDIO-3 Channel Electrocardiograph

  Class II

  FDA 510(k) K850454 Active Cleared 1 Mar 1985

• Galva-5-M

  Class II

  FDA 510(k) K954411 Active Cleared 28 Feb 1996

• Sinus Ac-Powered Muscle Stimulator

  Class II

  FDA 510(k) K850453 Active Cleared 7 May 1985

• Disposable Therapy Electrode

  Class II

  FDA 510(k) K924473 Active Cleared 19 May 1993

See all devices from Zimmer Elektromedizin GmbH →