Luteinizing Hormone (Lh) Ria

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K792000 ↗

FDA Product Code

CEP

Device Class

Class I

Regulation

21 CFR Part 862.1485

Advisory Committee

Clinical Chemistry

FDA Decision

SESE Substantially Equivalent

• Ferritin Ria Kit

  Class II

  FDA 510(k) K791860 Active Cleared 6 Dec 1979

• Progesterone Radioimmunoassay Kit

  Class I

  FDA 510(k) K791051 Active Cleared 24 Jul 1979

• Iridium 192 Wires & Pins

  Class II

  FDA 510(k) K771878 Active Cleared 27 Oct 1977

• Kits, Ria, Myoglobin, Human, Measurement

  Class II

  FDA 510(k) K780982 Active Cleared 22 Jun 1978

• Follicle Stimulating Hormone (Fsh) Kit

  Class I

  FDA 510(k) K792063 Active Cleared 20 Nov 1979

• Set, Oral Administration

  Class II

  FDA 510(k) K760251 Active Cleared 15 Sep 1976

See all devices from Cis Radiopharmaceuticals, Inc. →