Galva-5-M

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

510(k) Number

K954411 ↗

FDA Product Code

IPF

Device Class

Class II

Regulation

21 CFR Part 890.5850

Advisory Committee

Physical Medicine

FDA Decision

SN

• Galva 5-T

  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

• 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

• Sono 5

  Class II

  FDA 510(k) K952536 Active Cleared 5 Mar 1996

See all devices from Zimmer Elektromedizin GmbH →