Insulin Ria Kit

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K781285 ↗

FDA Product Code

CFP

Device Class

Class I

Regulation

21 CFR Part 862.1405

Advisory Committee

Clinical Chemistry

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. →