Model Em-2 Bioelectric Processor

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K830034 ↗

FDA Product Code

KZM

Device Class

Class II

Regulation

21 CFR Part 890.1375

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

• Monitor, Myo, Model J3

  Class II

  FDA 510(k) K770252 Active Cleared 18 Feb 1977

• Model EM-IR

  Class II

  FDA 510(k) K810528 Active Cleared 31 Mar 1981

• Testcorp Ra

  Class II

  FDA 510(k) K831364 Active Cleared 27 May 1983

• J4 Myo-Monitor

  Class II

  FDA 510(k) K842223 Active Cleared 19 Nov 1984

• Bns 40

  Class II

  FDA 510(k) K842224 Active Cleared 19 Nov 1984

• Electric Muscle Stimulator (K813533)

  Class II

  FDA 510(k) K813533 Active Cleared 5 Mar 1982

See all devices from Myo-Tronics Research, Inc. →