Mega Pulse Therapy Unit

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

510(k) Number

K841874 ↗

FDA Product Code

IMJ

Device Class

Class II

Regulation

21 CFR Part 890.5290

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

• Omnivac (Vacuum Electrode System)

  Class II

  FDA 510(k) K861039 Active Cleared 26 Sep 1986

• Omnistim III Interferential Therapy

  Class II

  FDA 510(k) K841278 Active Cleared 24 Apr 1984

• Modified Omnistim Electrical Muscle Stimulator

  Class II

  FDA 510(k) K874076 Active Cleared 4 Jan 1988

• G5 Apparatus T, K1, K3 & the President Model's

  Class I

  FDA 510(k) K850851 Active Cleared 25 Jun 1985

• Omnisound Therapy Unit

  Class II

  FDA 510(k) K843372 Active Cleared 18 Sep 1984

• Automove/Omnistim IV-Electrical Muscle Stimulator

  Class II

  FDA 510(k) K850850 Active Cleared 1 Jul 1985

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