Nordiclab Total Estriol Ria Test

No FDA recalls found in the data synced 12 Oct 2026.

510(k) Number

K792189 ↗

FDA Product Code

CGI

Device Class

Class I

Regulation

21 CFR Part 862.1265

Advisory Committee

Clinical Chemistry

FDA Decision

SESE Substantially Equivalent

• Nordiclab Progesterone Ria Test

  Class I

  FDA 510(k) K800922 Active Cleared 14 May 1980

• RIA Test, Nordiclab HPL

  Class II

  FDA 510(k) K782099 Active Cleared 10 Jan 1979

• Nordiclab Ferritin Irma Test

  Class II

  FDA 510(k) K801989 Active Cleared 16 Sep 1980

• Nordiclab Testosterone Ria Test

  Class I

  FDA 510(k) K800921 Active Cleared 14 May 1980

• Nordiclab Prostatic Acid Phosphatase Ria

  Class II

  FDA 510(k) K801988 Active Cleared 26 Sep 1980

• Nordiclab Estradiol Ria Test

  Class I

  FDA 510(k) K800920 Active Cleared 14 May 1980

See all devices from Nordiclab Intl. →