High Frequency Epilator Cb-2

No FDA recalls on record, checked 9 Oct 2026.

510(k) Number

K823674 ↗

FDA Product Code

KCW

Device Class

Class I

Regulation

21 CFR Part 878.5350

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• 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

• Md-2 Iontophoresis Unit

  Class II

  FDA 510(k) K895365 Active Cleared 26 Jun 1990

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