Md-2 Iontophoresis Unit

No FDA recalls on record, checked 10 Oct 2026.

510(k) Number

K895365 ↗

FDA Product Code

EGJ

Device Class

Class II

Regulation

21 CFR Part 890.5525

Advisory Committee

Physical Medicine

FDA Decision

SESD Substantially Equivalent — Deferred

• High Frequency Epilator Cb-2

  Class I

  FDA 510(k) K823674 Active Cleared 14 Jan 1983

• Model Cbx Epilator

  Class I

  FDA 510(k) K884079 Active Cleared 4 Oct 1988

• Model Se-5 Epilator

  Class I

  FDA 510(k) K893389 Active Cleared 5 Jun 1989

• Cb-7 Electronic Epilator

  Class I

  FDA 510(k) K871372 Active Cleared 28 Apr 1987

• Md-1A Galvanic Unit

  Class II

  FDA 510(k) K964208 Active Cleared 30 Apr 1997

• Electronic Epilator Ts-1

  Class I

  FDA 510(k) K843063 Active Cleared 26 Sep 1984

See all devices from R. A. Fischer Co. Corp. →