Aca Du Pont Urine Amphetamines (U Amp) Screen Meth

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

510(k) Number

K873622 ↗

FDA Product Code

DKZ

Device Class

Class II

Regulation

21 CFR Part 862.3100

Advisory Committee

Clinical Toxicology

FDA Decision

SESE Substantially Equivalent

• Aca Iron Calibrator

  Class II

  FDA 510(k) K771802 Active Cleared 25 Oct 1977

• Du Pont Tobramycin Assay Reagents

  Class II

  FDA 510(k) K850058 Active Cleared 18 Jan 1985

• Du Pont Xenolite(Tm) Radiation Protection Apparel

  Class I

  FDA 510(k) K896511 Active Cleared 22 Dec 1989

• Aca Carbon Dioxide Calibrator

  Class II

  FDA 510(k) K771801 Active Cleared 25 Oct 1977

• Du Pont Aca Plus Immunoasssay System Hcg Calibrato

  Class II

  FDA 510(k) K922696 Active Cleared 12 Aug 1992

• Du Pont Analyst Analytical Test Rotor:CHEM-14, Cali

  Class II

  FDA 510(k) K901017 Active Cleared 15 May 1990

See all devices from E.I. Dupont DE Nemours & Co., Inc. →