Cadwell 7200

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

510(k) Number

K800648 ↗

FDA Product Code

IKN

Device Class

Class II

Regulation

21 CFR Part 890.1375

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

• Promontory Stimulating Electrode

  Class II

  FDA 510(k) K895081 Active Cleared 9 Nov 1989

• Ten-20 Conductive Paste Gel

  Class II

  FDA 510(k) K933799 Active Cleared 27 May 1994

• Ground Plate Electrode

  Class II

  FDA 510(k) K933807 Active Cleared 26 Jul 1994

• Kilowin

  Class II

  FDA 510(k) K971214 Active Cleared 11 Jun 1998

• Lectron II Conductive Gel/Cadwell Electrode Gel

  Class II

  FDA 510(k) K933804 Active Cleared 22 Mar 1994

• Omni Prep Gel

  Class II

  FDA 510(k) K933797 Active Cleared 17 May 1994

See all devices from Cadwell Laboratories, Inc. →