Bowen Reuseable/Disposable Electrode

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K871325 ↗

FDA Product Code

DRX

Device Class

Class II

Regulation

21 CFR Part 870.2360

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Bowen Cannula

  Class I

  FDA 510(k) K863150 Active Cleared 5 Sep 1986

• Bowen Knot Passer

  Class I

  FDA 510(k) K863148 Active Cleared 5 Sep 1986

• Sternal Power Awl

  Class I

  FDA 510(k) K873766 Active Cleared 14 Nov 1988

• Morgan Arthroscopic Menesus & Synovial Rasp

  Class I

  FDA 510(k) K853601 Active Cleared 16 Sep 1985

• Disposable 45 Degree Shaver

  Class II

  FDA 510(k) K896538 Active Cleared 6 Dec 1989

• 45 Degree Shaver

  Class I

  FDA 510(k) K870882 Active Cleared 23 Mar 1987

See all devices from Bowen & Company, Inc. →