T4 Radioimmunoassay Kit

FDA 510(k) K802469 · American Diagnostic Corp.

Substantially Equivalent

510(k) numberK802469

Submission

Device name
T4 Radioimmunoassay Kit
Applicant
American Diagnostic Corp.
Mchenry, IL, US
Received
October 9, 1980
Decision date
November 12, 1980
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CDX – Radioimmunoassay, Total Thyroxine
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1700
Specialty
Clinical Chemistry

Other 510(k)s with product code CDX

510(k)DeviceApplicantDecision
K961490Elecsys T4 AssayCDX · Traditional Boehringer Mannheim Corp.06/13/1996SE
K954312Active Thyroxine RiaCDX · Traditional Diagnostic Systems Laboratories, Inc.10/07/1995SE
K943416Delfia Neonatal Thyroxine KitCDX · Traditional Wallac OY03/10/1995SE
K934384Axsym(Tm) Total T4CDX · Traditional Abbott Laboratories06/21/1994SE
K932980Total T4 Fpia Reagent Set/Calibrator #T-1039,T-116CDX · Traditional Sigma Diagnostics, Inc.10/18/1993SE
K933426Stratus(R) Total THYROXINE(T4) Fluor Enzyme ImmunoCDX · Traditional Baxter Diagnostics, Inc.08/26/1993SE
K931295Iq TT4 AssayCDX · Traditional Becton Dickinson Advanced Diagnostics07/20/1993SE
K926563Autobead(Tm) T4 Enzyme Immunoassay Test KitCDX · Traditional Bio-Chem Laboratory Systems, Inc.03/18/1993SE
K925110Abbott Imx T4CDX · Traditional Abbott Laboratories01/26/1993SE
K925109Abbott Tdx/Tdxflx TT4CDX · Traditional Abbott Laboratories01/04/1993SE

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Questions and answers

When was T4 Radioimmunoassay Kit cleared by the FDA?

T4 Radioimmunoassay Kit (K802469) received a 510(k) decision of Substantially Equivalent on November 12, 1980, 34 days after the submission was received.

What is the product code of K802469?

The FDA product code is CDX – Radioimmunoassay, Total Thyroxine, a Class II (moderate risk) device regulated under 21 CFR 862.1700.