Diamond Medical, Inc. Model Dm 800

No FDA recalls on record, checked 11 Oct 2026.

510(k) Number

K874709 ↗

FDA Product Code

FFT

Device Class

Class I

Regulation

21 CFR Part 876.1400

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

• Diamond Medical, Inc. Model Dm 600

  Class I

  FDA 510(k) K874710 Active Cleared 8 Feb 1988

• Dmi Blod Gas Analyzer/Cartridge

  Class II

  FDA 510(k) K915087 Active Cleared 8 Jan 1992

• Diamond Medical, Inc., Model Dm 700

  Class I

  FDA 510(k) K863298 Active Cleared 17 Mar 1987

• Model Iso-2001 Univ. Patient Isolation Circuit

  Class I

  FDA 510(k) K875369 Active Cleared 5 Feb 1988

• DMI Blood Gas Analyzer/Cartridge

  Class II

  FDA 510(k) K924758 Active Cleared 3 Dec 1992