Immunoreactive Estriol Ria Kit

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K802754 ↗

FDA Product Code

CGI

Device Class

Class I

Regulation

21 CFR Part 862.1265

Advisory Committee

Clinical Chemistry

FDA Decision

SESE Substantially Equivalent

• MRI Gentamicin Ria Kit

  Class II

  FDA 510(k) K812394 Active Cleared 8 Sep 1981

• Trypsin Ria Kit

  Class I

  FDA 510(k) K861097 Active Cleared 29 May 1986

• MR1 Follitropin Ria Kit

  Class I

  FDA 510(k) K820740 Active Cleared 6 Apr 1982

• MRI Tobramycin Ria Kit

  Class II

  FDA 510(k) K813516 Active Cleared 29 Dec 1981

• MRI HCG-Beta RIA Kit Cat. #MR-10100

  Class II

  FDA 510(k) K801491 Active Cleared 13 Aug 1980

• MR1 Lutropin Ria Kit

  Class I

  FDA 510(k) K820741 Active Cleared 14 Apr 1982

See all devices from Microanalytic Research, Inc. →