Dupont Dimension C-Reactive Protein Method

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

510(k) Number

K945280 ↗

FDA Product Code

DCK

Device Class

Class II

Regulation

21 CFR Part 866.5270

Advisory Committee

Immunology

FDA Decision

SESE Substantially Equivalent

• Urinary Albumin Test Pack

  Class I

  FDA 510(k) K936202 Active Cleared 9 May 1994

• Creatine Kinase Method

  Class II

  FDA 510(k) K941584 Active Cleared 6 Jul 1994

• Dupont APC Blood Collection Container With Thromboplastin

  Class II

  FDA 510(k) K942241 Active Cleared 18 Aug 1994

• Du Pont Identification Camera

  Class I

  FDA 510(k) K910354 Active Cleared 29 Mar 1991

• Dupont Aca Plus Fsh/Lh/Prolactin Calibrator

  Class II

  FDA 510(k) K941219 Active Cleared 9 Aug 1994

• Lipase Flex Reagent Cartridge

  Class I

  FDA 510(k) K952816 Active Cleared 20 Jul 1995

See all devices from Dupont Medical Products →