Thyroxine Radioimmunoassay Kit

FDA 510(k) K801105 · Calbiochem-Behring Corp.

Substantially Equivalent

510(k) numberK801105

Submission

Device name
Thyroxine Radioimmunoassay Kit
Applicant
Calbiochem-Behring Corp.
Mchenry, IL, US
Received
May 9, 1980
Decision date
June 9, 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

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K961490Elecsys T4 AssayCDX · Traditional Boehringer Mannheim Corp.06/13/1996SE
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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 Thyroxine Radioimmunoassay Kit cleared by the FDA?

Thyroxine Radioimmunoassay Kit (K801105) received a 510(k) decision of Substantially Equivalent on June 9, 1980, 31 days after the submission was received.

What is the product code of K801105?

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