Opticoat T3 Eia Kit

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K981824 ↗

FDA Product Code

CDP

Device Class

Class II

Regulation

21 CFR Part 862.1710

Advisory Committee

Clinical Chemistry

FDA Decision

SESE Substantially Equivalent

• Cortisol Clasp-Bead Eia Kit

  Class II

  FDA 510(k) K895407 Active Cleared 19 Oct 1989

• Progesterone Direct Ria Kit-Radioimm

  Class I

  FDA 510(k) K841333 Active Cleared 2 May 1984

• Tbg 125I Ria Kit, Radioimmuno. of Serum Thyroxine

  Class II

  FDA 510(k) K883765 Active Cleared 31 Oct 1988

• Estradiol Direct Ria Kit

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  FDA 510(k) K851540 Active Cleared 6 Jun 1985

• Aldosterone Direct Ria Kit

  Class II

  FDA 510(k) K854876 Active Cleared 17 Mar 1986

• Opticoat T4 Eia Kit

  Class II

  FDA 510(k) K982298 Active Cleared 3 Feb 1999

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