Liquisol Digoxin Ria Test Kit

No FDA recalls on record, checked 10 Oct 2026.

510(k) Number

K780207 ↗

FDA Product Code

DON

Device Class

Class II

Regulation

21 CFR Part 862.3320

Advisory Committee

Clinical Toxicology

FDA Decision

SESE Substantially Equivalent

• Adrenocorticotropin Radio-Immunoassay

  Class II

  FDA 510(k) K831826 Active Cleared 18 Jul 1983

• Liquisol Cortisol Ria Test Kit

  Not classified

  FDA 510(k) K790250 Active Cleared 4 Apr 1979

• Liquisol Testosterone Radioimm. Test Kit

  Class I

  FDA 510(k) K802661 Active Cleared 10 Dec 1980

• Analyzeo, Plasma, Blood, Colysagraph

  Class II

  FDA 510(k) K770606 Active Cleared 6 May 1977

• Liquisol Progesterone Radioimmuno

  Class I

  FDA 510(k) K820686 Active Cleared 1 Apr 1982

• Ria Test Kit Sys. Damon Kiquisol Free

  Class II

  FDA 510(k) K781012 Active Cleared 27 Jul 1978

See all devices from Damon Corp. →