Ria Test Kit Sys. Damon Kiquisol Free

No FDA recalls on record, checked 10 Oct 2026.

510(k) Number

K781012 ↗

FDA Product Code

CEC

Device Class

Class II

Regulation

21 CFR Part 862.1695

Advisory Committee

Clinical Chemistry

FDA Decision

SESE Substantially Equivalent

• Adrenocorticotropin Radio-Immunoassay

  Class II

  FDA 510(k) K831826 Active Cleared 18 Jul 1983

• Liquisol Digoxin Ria Test Kit

  Class II

  FDA 510(k) K780207 Active Cleared 23 Feb 1978

• 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

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