Human Placental Lactogen Radioimmuno-

No FDA recalls on record, checked 11 Oct 2026.

510(k) Number

K810625 ↗

FDA Product Code

DHI

Device Class

Class I

Regulation

21 CFR Part 866.5065

Advisory Committee

Immunology

FDA Decision

SESE Substantially Equivalent

• Estradiol Ria Kit

  Class I

  FDA 510(k) K790679 Active Cleared 23 May 1979

• Estriol Radioimmunoassay Test Kit

  Class I

  FDA 510(k) K810695 Active Cleared 31 Mar 1981

• Pap-Check Ria Kit

  Class II

  FDA 510(k) K792043 Active Cleared 30 Oct 1979

• Progesterone

  Class I

  FDA 510(k) K790440 Active Cleared 3 May 1979

• Preg-Stat RIA Kit

  Class II

  FDA 510(k) K781733 Active Cleared 20 Dec 1978

• RIA Kit, Neonatal T4

  Class II

  FDA 510(k) K782103 Active Cleared 17 Jan 1979

See all devices from Serono Laboratories, Inc. →